Abstract: A flexible stick of a bow exercise device includes a base and a top cap, and a first and second flexible plates are connected between the base and the top cap. Two ends of the first flexible plate are respectively connected to the base and the top cap. A first end of the second flexible plate is connected to the base and a second end of the second flexible plate is movably inserted in a slot defined in the top cap. A gap is defined between the first and second flexible plates when the stick is not bent. The top cap can be removed from the two flexible plates and the second flexible plate can be replaced with another one with different flexibility.

Abstract: Exercise machines for the leg muscles using separate machines for the biceps femoris and quadriceps and with the biceps femoris machines configured so that the muscle attachment below the knee is the “origin” and the muscle attachment on the upper leg and hip bone is the “insertion”.

Abstract: A cover structure of a machine tool with a simple structure which improves work efficiency by minimizing an opening portion. An opening portion is defined in a reverse concave shape at one lateral side of a cover. The opening portion includes two tool passing portions and a turning permission portion connecting the tool passing portions. A tool T which is held by an exchange arm passes through each tool passing portion. On the other hand, a rotation base portion of the exchange arm passes through the turning permission portion. While each tool passing portion is closed by a door, the turning permission portion is closed by a closing cover including a turning cover and a slide cover.

Abstract: A spindle (5) has a chuck (9) provided on a distal end (5a) thereof for chucking a tool (11), and a nut (13) screwed to the distal end (5a) and rotatable for tightening and loosening the chucking. The spindle (5) is positioned relative to a nut loosening station provided with a nut loosening driver (43) for driving the nut (13) to rotate in a loosening direction, the nut (13) is loosened by the nut loosening driver (43) to remove from the chuck (9) a first tool (11) to be replaced with a second tool (11), the spindle (5) is positioned relative to a nut tightening station provided with a nut tightening driver (41) for driving the nut (13) to rotate in a tightening direction, and the nut (13) is driven by the nut tightening driver (41) to tight-chuck the second tool (11).

Abstract: A tool changing device for a machine tool with at least one tool carrier is proposed, which comprises at least one transit station, into which a tool is introducable in an inward transit direction and is extractable in an outward transit direction, wherein, at the transit station, the tool is at least one of detachable from the assigned tool carrier and fixable to the tool carrier provided.

Abstract: A circular-shaped metal structure is fabricated by plastic-working and has a wall thickness in the range of 0.03 mm to 0.09 mm both inclusive. A film composed of one of (a) silicon and fluorocarbon resin and (b) copper is coated on a surface of the circular-shaped metal structure.

Abstract: A screw conveyor intended and formed for use in a decanter centrifuge for separation of solid particles from a fluid compound, comprising a central body, at least one conveyor thread and at least one baffle bridging a flow path formed between different parts of the conveyor thread. The screw conveyor has at least two originally separate parts, each of which comprises a portion of said conveyor thread and which are kept together axially. The baffle constitutes a separate member arranged to be kept in place between said parts of the screw conveyor, when these parts are kept together axially, and has a portion which forms a part of the conveyor thread in an area where the conveyor thread intersects with and extends past the baffle.

Abstract: An automated system for loading low dose radioisotope seeds into a plurality of implant needles is comprised of a loading station into which a replaceable cartridge may be positioned. The cartridge is preloaded with a plurality of radioisotope seeds and a plurality of spacers. The cartridge has at least one aperture and preferably the radioisotope seeds and spacers are loaded around the periphery of a rotatable drum within the cartridge. The loading station has a cartridge receiving structure and an automated motion control system. When the cartridge is positioned in the cartridge receiving structure, the automated motion control system preferably drives a pair of stepper motors within the cartridge, one for rotating the rotatable drum and one for sliding a pushrod to selectively eject radioisotope seeds and spacers from the cartridge into each of a plurality of implant needles positioned so as to receive the radioisotopes seeds and spacers within the implant needle.

Abstract: The invention relates to a device and method for inserting a needle in an animal body for effecting radiation therapy in the body, including a template for positioning the needles to be inserted, needle drive structure for drive a needle through said template towards a desired location in the body, and real-time imaging structure for creating and presenting an image of the desired location and the position of said needle during the insertion of said needle. Due to the fact that the bevelled tip of a hollow needle cause the needle to diverge away from the “line of insertion or movement” and away from the actual desired position in the animal body adversely affecting the dosimetry quality of the implanted seeds a more accurate insertion of the needle is required. According to the invention the device is provided with adjusting structure for adjusting a movement of said needle towards said desired location during insertion.

Abstract: The present invention is a cardiac-assist device and technique used to maintain a patient's cardiac output when normal cardiac output is insufficient. Blood is removed from a selected ventricle using an arterial or venous side approach. The use of a right side approach reduces the amount of work required and reduces the number of foreign objects present within the left side of the heart and associated blood transferring conduits. The device of the invention includes a flexible catheter positionable within the patient's body. An external assist mechanism connected to one end of the flexible catheter receives blood from the arterial circulation and includes a pumping membrane. A flexible cannula is connected for reinfusing blood. A control console is provided for alternately supplying vacuum and pressure to the pumping membrane. A synchronizing means varies inflation and deflation in synchrony with the cardiac cycle of a patient.

Abstract: A balloon catheter has a balloon membrane, a tip connected to the distal end of the balloon membrane and an outer tube connected to the proximal end of the balloon membrane for supplying a medium for inflating and deflating the balloon membrane. A pressure sensor, such as a fiber optic sensor, may be mounted in a pocket in the tip. The pocket may be filled with a flexible substance which both communicates pressure to and protects the pressure sensor. A membrane may overlie the pocket to prevent leakage of the flexible substance therefrom.

Abstract: The invention concerns a surgical device forming a surgical prosthesis. This device is characterized in that it contains at least one first sling (20), at least one first traction component (30), and at least one first fixation or anchoring system (40), designed to work in concert with at least said first traction component (30), which includes a cage-forming device (42), the upper end (43) of which is fitted with a sliding component (46) which makes it easier to pull on the traction component (30) which acts on the sling (20), so that said pulling effects translation of one end of the sling (20). The device is preferably intended for the treatment of urinary incontinence in female mammals, in particular the human female.

Abstract: A delivery system for delivering and mounting a cardiac harness on a heart including an elongate body having a proximal portion and a distal portion. The body includes a cavity sized to contain the cardiac harness in a compacted configuration and also includes a plurality of elongate push rods movable with respect to the body. The cardiac harness is releasably connected to the push rods such that, advancement of the push rods in a distal direction moves the cardiac harness from a compacted configuration, within the cavity, to an expanded configuration, outside the cavity. The push rods are configured to have varying stiffness along their length to provide sufficient flexibility to bend up to 90° to advance the cardiac harness onto the heart.

Abstract: A device for positioning at least one optical component inside an endoscopic system has a housing through which an optical axis of the endoscopic system extends and in which the at least one optical component is arranged. The at least one optical component can be pivoted into the beam path and back out of the beam path about a pivot axis extending substantially parallel to a longitudinal axis of the housing, the at least one optical component being arranged on a support which is pivotable about the pivot axis. A smallest distance of an inside wall of the housing from the pivot axis is smaller than a greatest distance of the pivot axis to an outer edge of the at least one optical component.

Abstract: A capsule endoscope includes a capsule portion. The capsule portion includes at least an observation optical unit having an image pick-up element and an optical lens that forms an objective optical system, an illuminating unit having an illuminating substrate, an electroluminescence light source, and a light-emitting control circuit, a peripheral-circuit part which forms various circuits having a signal processing circuit, a receiving and transmitting circuit, and a control circuit, and a power source unit which supplies power to the observation optical unit, the illuminating unit, and the peripheral-circuit part.

Abstract: A compact, low-profile surgical retractor (100) avoids the need for a bulky frame. The retractor includes retractor blade components (110, 120, 130, 140, 150, 160) joined pivotally. A cable (170) is guided by each retractor blade component. A winding mechanism (180), such as a spool, is carried by one of the retractor blade components (120) for winding up the cable to cause the retractor blade components to transition from a closed position to an open position. The winding mechanism may be actuated by a detachable handle (200). The retractor blade components may be unitary, injection-molded pieces. The retractor blade components may be fixed pivotally, such as by pins, or pivotally joined by living hinges. A less-invasive surgical method is also provided in which the retractor is inserted into the body through an incision.

Abstract: A system for providing a home health care service includes a health care center, a service recipient device, and the Internet that connects these components. The health care center: is constructed on the Internet; includes a database for registering personal data that are necessary for the health care of registered at-home patients as basic health care data and storing measurement data that are provided from at-home patients over the course of time; and has the functions of inferring the health conditions of at-home patients based on the measurement data and the basic health care data, and offering appropriate services necessary for inferred health conditions. The service recipient device includes a biosensor and a signal processor. The biosensor detects chemical components contained in a substance that is discharged from the human body and converts detected values to electrical signals at the point of discharge.

Abstract: A method and a device are used for determining a characteristic value for the perfusion of modified, in particular pigmented tissue regions in organs of living beings, for example the skin. By means of a laser flowmeter, a first volumetric flow rate and a second volumetric flow rate of the blood are determined at a first measurement point and at a second measurement point, respectively within the modified tissue region and within the surrounding, unmodified tissue region, in each case as a measurement profile of a volumetric flow rate signal as a function of time. A wavelet analysis of each of the measurement profiles is then carried out as a three-dimensional representation of the signal intensity over a frequency or scaling axis and time.

Abstract: An ultrasonic system useful for providing imaging, therapy and temperature monitoring generally comprises an acoustic transducer assembly configured to enable the ultrasound system to perform the imaging, therapy and temperature monitoring functions. The acoustic transducer assembly comprises a single transducer that is operatively connected to an imaging subsystem, a therapy subsystem and a temperature monitoring subsystem. The ultrasound system may also include a display for imaging and temperature monitoring functions. An exemplary single transducer is configured such that when connected to the subsystems, the imaging subsystem can generate an image of a treatment region on the display, the therapy subsystem can generate high power acoustic energy to heat the treatment region, and the temperature monitoring subsystem can map and monitor the temperature of the treatment region and display the temperature on the display, all through the use of the single transducer.

Abstract: A medical ultrasound viewing system for processing a sequence of three-dimensional (3-D) ultrasound images far performing a quantitative estimation of a flow through a body organ comprising means for performing steps of acquiring a sequence of 3D color flow images, of said flow; assessing the flow velocity values in the 3D images, constructing isovelocity surfaces (6) by segmentation of the flow velocity values; computing the volume (Vol) delimited by the isovelocity surfaces; and using the flow velocity value (V) and the volume (Vol) computed from a segmented surface for computing the surface of an orifice (3) of the organ through which the flow propagates.

Abstract: An ultrasonically visible solid device for inserting into a non-gas target medium comprises an echogenic surface having structures entrapping gas when the device is in the target medium, the entrapped gas causing the device to be ultrasonically visible, wherein the gas-entrapping structures are covered with a flexible overcoat that does not significantly reduce the compressibility of the gas trapped in the structures.

Abstract: A pulse wave measuring apparatus extracts a direct current component from a pressure value obtained from a sensor pressure, and defines the pressurization force of the cuff as the optimum pressurization force when that direct current component is stable. Following determination of the optimum pressurization force, the pulse wave measuring apparatus monitors whether the direct current component obtained from the pressure sensor is optimum or not, and adjusts the pressure, when not. By determining the rising sharpness of the peak and waveform distortion in the sphygmographic waveform, determination is made whether the pressurization force of the cuff is appropriate or not to carry out further adjustment of pressure, as necessary.

Abstract: A method for implanting a medical device between tissue comprises the steps of providing a catheter having a body and a distal end thereof wherein the catheter includes an implantable device comprising a housing having a proximal end and a distal end and a longitudinal axis. The implantable device further includes a first set of anchoring members operatively connected to the proximal end of the housing and a second set of anchoring members operatively connected to the distal end of the housing. Both sets of anchoring members are movable between a collapsed position and a deployed position. Each set of anchoring members includes ring members connected to a housing of the device. Further steps of the method include inserting the distal end of the catheter into tissue and disposing the medical device at least partially from the distal end of the catheter.

Abstract: An exercise expenditure monitor device and method for monitoring a user's caloric expenditure at exercise, the exercise expenditure monitor device including a heartbeat sensing device for detecting heart rate of the user, a reference storage unit for storing a standard heart rate and a reference heart rate of the user at rest mode, an individual physiology database for storing data of physiology weighted value and a set of individual physiological parameters inputted by the user including sex, age and weight, each set of individual physiological parameters corresponding to a physiology weighted value, a calculating unit which calculates a general caloric expenditure of the user according to an algorithm including dividing the heart rate difference between the exercise heart rate and the reference heart rate by the reference heart rate and multiplying by the physiology weighted value.

Abstract: Implantable devices and methods of use are disclosed for marking the location of a biopsy or surgery for the purpose of identification. The methods include providing a biodegradable radiodense implant and taking a tissue sample from a biopsy site within a breast of a patient. The biodegradable implant is then positioned at the biopsy site. The tissue sample is tested and the biopsy site is then relocated. In one embodiment, the entire implant is radiodense. In another embodiment, the entire implant is biodegradable. Methods of using a biodegradable implant having a radiodense material and a biodegradable implant that is visible using an imaging system are also included.

Abstract: A device for encapsulating tissue specimens includes a wand assembly, a sheath, and a guide assembly. The guide assembly pulls, draws, or otherwise moves the sheath about the tissue specimen. The wand assembly is disposed proximate to the tissue specimen, typically either adjacent or through the specimen. The guide assembly has sheath deployment members that are disposed about the tissue specimen. The sheath, which is attached to ends of the sheath deployment members and the wand assembly, is drawn over the tissue specimen as the sheath deployment members are pushed or pulled. In another aspect of the device, the guide assembly is an arm or a housing that rotates about the tissue specimen. The sheath, which is secured at one end to the guide assembly and at another end to the wand assembly, is drawn over the tissue specimen as the guide assembly rotates.

Abstract: An automatic tissue sampling apparatus for use with a biopsy needle set having an inner needle and an outer cannula is provided. The apparatus includes a slidably disposed, spring-biased carrier for each of the inner needle and cannula A cocking mechanism is operable to sequentially move the first carrier to its cocked position and the second carrier to its cocked position. The cocking mechanism includes a manually operated cocking lever positioned outside the housing for single handed manipulation while holding the housing. A force transmission mechanism is operably coupled between the cocking lever and the carriers and configured so that the force required to manually depress the cocking lever to force the springs to the cocked positions does not increase as the springs are compressed.

Abstract: A medical instrument including a ductal access device comprising a low profile, ergonomic manifold hub usable to introduce fluids into a breast duct and collect ductal fluid samples including ductal epithelial cells and clumps of ductal epithelial cells from within a breast duct. The ductal access device also comprises an elongated access catheter having a distal end, one lumen and dimensions which permit introduction of the distal end through a ductal orifice so that a distal end of the catheter may be positioned distal to the ductal sphincter of a human breast. The medical instrument may also include at least one spacing member for adjustably positioning the manifold hub a desired distance above the surface of the nipple. The spacing member may control the insertion depth of the catheter into the duct. The medical instrument may also include at least one member for anchoring the device to the breast.

Abstract: An apparatus for deploying a needle within a lumen is provided. The apparatus includes a housing having a threaded bushing radially disposed therein. The bushing rigidly couples with a nose cone having a guide tip disposed at an end opposite the bushing for penetrating an arterial wall of a lumen. During operation, a user incrementally advances the bushing within the housing, thereby incrementally advancing the guide tip into the lumen. The nose cone also includes a flex guide having a slot configuration which couples with the guide tip which deploys into the lumen along with the guide tip.

Abstract: The suction cup is placed in sealing contact on the anterior side of the torso. A partial vacuum can be applied to the body by the suction cup. The suction cup is composed at least in part of soft elastic materials. It is provided with inner flanks that flare toward the body when under atmospheric pressure. The suction cup bears with lateral body-fitting portions on each side of the sternum, with an upper body-fitting portion on the upper region of the sternum and with a lower body-fitting on the lower region or below the sternum. The deformability of the suction cup varies over its circumference. At least the upper, lower or one of the lateral body-fitting portions have different deformabilities.

Abstract: Systems and methods apply audible acoustic energy to cause vasodilation and/or to increase tissue perfusion.

Abstract: The present invention provides a hand-held massage assembly that is modular and allows a user the option of using a roller mechanized massager with or without a handle. In accordance with an embodiment of the present invention, the hand-held massage assembly includes a roller mechanized massager having an electro-mechanical connection. A handle is connectable to the electro-mechanical connection on the roller mechanized massager by a first electro-mechanical connection at one end thereof. The handle also has a second electro-mechanical connection at an opposite end. The first electro-mechanical connection and second electro-mechanical connection of the handle are electrically coupled to each other. A power cord having an electro-mechanical connection is coupled to the second electro-mechanical connection on the handle.

Abstract: A method and apparatus for aerating a fracture sight that employs a membrane or covering that wraps and seals the outside of a breathable, orthopedic cast and typically includes an array of spaced apart protrusions on an inside surface to facilitate generally even airflow, thereby providing comfort and/or improved hygiene for the patient when an air moving device is connected to the apparatus and the air moving device is powered on.

Abstract: A tennis elbow support comprising a main body having an opening and a tendon pad having a pad base and a raised portion that projects from the pad base. The tendon pad is inserted into the opening so that the raised portion projects outwardly from a bottom surface of the main body. The main body can be releasably secured in a substantially circular configuration so that the support can be placed around the forearm of a user and the tennis elbow support can be tightened around the arm of the user with tendon pad in contact with the arm so that straight-line pressure is applied across the extensor muscle and tendon.

Abstract: A method and apparatus for preventing and treating septicemia in patient blood is provided. The extracorporeal system includes an antimicrobial device to inactivate at least 99% of bloodborne microorganisms, a hemoconcentrator/filtration unit to remove approximately 50–75% of target molecules from the patient blood and a filter unit to remove target molecules from patient blood from the sieved plasma filtrate. Target molecules are produced by microorganisms, as well as by the patient's cells. These molecules include endotoxins from Gram negative bacteria, exotoxins from Gram negative and Gram positive bacteria, as well as RAP protein mediator from Staphylococcus aureus, and cell mediators such as tumor necrosis factor-alpha, and interleukin 1-beta, interleukin 6, complement proteins C3a and C5a, and bradykinin.

Abstract: A bypass conduit assembly is placed in a hollow body organ to route food and liquids past the hollow body organ. A flexible tubular member extends from a narrowed section through the hollow body organ and into either the pylorus or intestines. The tubular member is connected to tissue by fasteners such as clips, staples or stents.

Abstract: A cylindrical elongate body having proximal and distal ends and enclosing two similar longitudinally extending lumens separated by a septum and a further lumen within the septum. A convergently tapered tip extending from the distal end of the body defines part of the further lumen that extends distally beyond the longitudinally extending lumens, while a connector at the proximal end of the body couples plural access tubes in fluid communication with respective individual of the lumens. Openings providing access to each of the longitudinally extending lumens are spaced from one another longitudinally along the body. The further lumen terminates at an opening at the distal end of the tip. The longitudinally extending lumens are blocked immediately distally of the openings.

Abstract: A method and apparatus for reducing the workload of titrating drug to effect while leaving clinician users in control of a related procedure is described. A drug delivery device is controlled to achieve a target drug concentration at a selected site in the patient or a predetermined infusion rate waveform. The time profile of the target drug concentration or a predetermined infusion rate waveform is controlled by a drug state model that uses clinical heuristics to implement safe, pre-defined changes in the target drug concentration or infusion rate and user-commanded changes in target drug concentration or infusion rate. The invention allows time to assess the response of the patient to changes in drug level by making small incremental and conservative changes in drug level over time.

Abstract: A catheter is insertable into a vessel within a mammalian body. The catheter includes a tubular body, at least one channel extending along the tubular body, and a central lumen. The tubular body includes an exterior surface, a first end and a second end, and defines a length between the first end and the second end. The channel passes between a first opening and a second opening and includes a slot in the tubular body between the channel and the exterior surface of the tubular body such that a tubular member can be passed between the channel and the exterior surface. The slot extends from the first opening to the second opening and includes a pair of edges. The central lumen extends along the tubular body at least for a portion of the length of the tubular body.

Abstract: When the injection device is applied to a patient's skin and a plunger is pressed, the entire syringe and a carrier move forwards in relation to a barrel such that ribs on the carrier snap past a rib on a shroud. The syringe is arrested by flanges coming up against the rib, and a spring is compressed and a needle is fully projected. Further pressing on the plunger ejects the dose. The needle shroud is kept at the rearward position by its firm engagement around the injection area. On withdrawal of the device, the shroud is pushed forwards by the spring to protect the needle. This draws fingers through gaps in the ribs, the fingers being forced to bend towards the fingers as the divergence takes effect.

Abstract: An apparatus for treating pneumothorax and/or hemothorax that does not require the assembly of parts and can be used by medical personnel with minimal experience and training in treating these conditions. The apparatus comprises a trocar obturator unit comprising a stylet having a point for puncturing the chest or other body cavity, and a stopper integrally attached to the stylet. The catheter assembly is comprised of a tube dimensioned to receive the stylet and a hub integrally attached to the distal end of the catheter assembly for receiving the stopper. The one-way valve composed of a pliable material covers the hub. The lumen of the one-way valve is continuous with the lumens of the tube and the hub of the catheter assembly. The trocar obturator unit also includes a pull handle for safely removing the trocar obturator unit from the catheter assembly in accordance with the method of the invention.

Abstract: Provided is a non-coring needle for venous access implantatable port. In one embodiment the non-coring needle comprises a puncturing assembly comprising two wings having a central sleeve, an L-shaped needle coupled to the sleeve, the needle including an annular groove or enlargement on its bent portion, and a plastic tubing coupled to the sleeve; and a syringe barrel comprising an internal chamber having a forward opening, and an elongate slot formed on the syringe barrel and being in communication with the chamber. The groove or enlargement is located at a first dent of the slot when the needle is concealed in the chamber in a non-use position, the groove or enlargement is located at a forward second dent of the slot when the needle is fully extended from the opening for use, and the groove or enlargement is permanently locked at a rear triangular recess of the slot when the needle is fully retracted into the chamber.

Abstract: An ophthalmic laser treatment apparatus which irradiates a laser beam to a patient's eye to be treated is disclosed. The apparatus includes: a first optical fiber which delivers a first laser beam emitted from a first laser source; a first light delivery optical system which forms an image of an emission end surface of the first optical fiber on the affected part of the eye in a predetermined first spot size being in a range of 50 ?m to 1000 ?m; a second optical fiber which delivers a second laser beam emitted from a second laser source; and a second light delivery optical system which forms an image of an emission end surface of the second optical fiber on the affected part of the eye in a predetermined second spot size in a range of 500 ?m to 7000 ?m.

Abstract: These and other objects of the present invention are achieved in a method for creating a desired tissue effect. An RF electrode is provided that includes a conductive portion. The RF electrode is coupled to a fluid delivery member that delivers a cooling fluidic medium to a back surface of the RF electrode. A dielectric is positioned on a skin surface. The RF electrode is coupled with the dielectric. RF energy is delivered from the RF electrode and the dielectric to the skin surface.

Abstract: A catheter or lead having electrically conductive traces and external electrical contacts. Each trace may be in electrical connection with one or more external electrical contacts. More specifically, each trace is typically electrically connected to a single contact. The traces and contacts may assist in diagnosis and/or detection of bio-electrical signals emitted by organs, and may transmit such signals to a connector or diagnostic device affixed to the catheter. The external electrical contacts may detect bioelectric energy or may deliver electrical energy to a target site.

Abstract: An ablation device includes a cannula having a distal end and a lumen, an array of electrodes deployable from within the lumen, each of the electrodes having a first configuration when inside the lumen, and a second configuration when unconfined outside the lumen, the electrodes having respective distal ends that point at least partially towards a distal direction when deployed, and an operative electrode secured to the distal end of the cannula. In one embodiment, the operative electrode has a shape that is different from the array of electrodes. In another embodiment, the operative electrode is not retractable within the lumen.

Abstract: A device and method of using the device to access a desired tissue site within a patient's body and separating a tissue specimen from the tissue site suitable for evaluation. The device includes a probe member having an arcuate tissue-cutting RF powered electrode secured to and distally spaced from the distal end of the probe and a small dimensioned distal extremity which when an inner lumen thereof is subjected to a vacuum, secured tissue for the specimen to the surface of the distal extremity. A circular tissue-cutting blade preferably secured to the distal end of a supporting tube is configured to rotate and move longitudinally along the shaft of the probe member effective to sever a tissue specimen from tissue secured to the surface of the distal extremity of the probe member. The supporting tube covers the separated specimen, and may be disposed within an accessing cannula.

Abstract: Devices and methods for a minimally invasive procedure for cutting tissue are disclosed. The device generally includes a probe with a distal exit at an exit angle relative to the probe, a cutting loop with shape memory having a preconfigured shape, and a loop securing mechanism to secure the cutting loop in a penetrating configuration and to release the cutting loop into a cutting configuration. The cutting loop is generally within a profile of the probe in the penetrating configuration. In the cutting configuration, the cutting loop extends through the cutting loop exit and generally returns to the preconfigured shape at a cutting angle generally defined by the exit angle. The cutting loop securing mechanism may be, for example, a cover slidable over the probe, a slidable member extending from a distal tip of the probe, or a groove defined in the probe proximal to the cutting loop exit.

Abstract: Systems for spinal stabilization and fixation replace, reconstruct or augment the spinal ligamentous and/or bony tissues resected during surgical procedures. The spinal stabilization system includes at least an implant configured to span the intervertebral disc space with at least one of its ends attached to a respective vertebral body by at least one anchor. The system has a low profile conformable to the spinal anatomy.

Abstract: The invention relates to a cervical vertebra plate (10) for osteosynthesis, having two receiving openings for the screw heads (18) of bone screws (16) in order to secure the cervical vertebra plate to two cervical vertebrae. The receiving openings have grooves (22) in the distal region on the periphery thereof and the depth of the grooves increases from a proximal to a distal end. The invention also relates to a bone screw (18) comprising a screw head (16) and a screw shank. The screw head comprises grooves (34) on the outer periphery thereof and the depth of the grooves varies along the length thereof.