Abstract: A power system, for powering a surgical instrument including an end effector and a motor configured to generate at least one motion to effectuate the end effector, includes a primary power source configured to supply a first power to operate the surgical instrument, wherein the primary power source is detachable from the surgical instrument, a secondary power source configured to supply a second power to operate the surgical instrument when the primary power source is detached from the surgical instrument, wherein the secondary power source is rechargeable, and wherein the primary power source is configured to charge the secondary power system, and a power management circuit configured to selectively transmit the first power from the primary power source and the secondary power from the secondary power source to operate the surgical instrument.

Abstract: Circular stapling instruments and anvil assemblies. The anvil assemblies may have collapsible anvil support members that may be inserted through an opening in a patient and then expanded to be attached to an anvil plate assembly that has a staple-forming surface thereon. The anvil support member is attachable to the anvil plate assembly in such a way that when the anvil assembly is coupled to the stapling head of a circular stapler, the staple-forming surface is in substantial registry with the staples supported in the stapling head. A variety of different anvil support members and anvil plate assemblies are disclosed.

Abstract: A surgical instrument system comprising a handle, a motor, a control system, an elongate shaft, a first unfired end effector configured to releasably attach to the elongate shaft, a second unfired end effector configured to releasably attach to the elongate shaft in lieu of the first end effector is disclosed. The first end effector comprises a stored datum. The second end effector does not comprise any stored datum. The control system is configured to identify the first end effector via the stored datum when the first end effector is attached to the elongate shaft and supply the motor with a first operating parameter based on the stored datum. The control system is further configured to detect an absence of any stored datum when the second end effector is attached to the elongate shaft and supply the motor with a second operating parameter based on the absence of any stored datum.

Abstract: A staple cartridge is disclosed. The staple cartridge can include a cartridge body, a plurality of staples, and an implantable layer. The implantable layer can include an inner portion, an outer portion positioned at least partially around the inner portion, and a plurality of passages formed through the outer portion toward the inner portion. The implantable layer can be porous. An implantable layer can include an outer portion including a plurality of fibers. A method of forming an implantable layer for use with a surgical stapler is also disclosed. The method can include forming at least one passage through an outer surface toward an inner portion of the implantable layer.

Abstract: A surgical instrument system can comprise a surgical instrument, a first end effector, and a second end effector, wherein the end effectors are attachable to the surgical instrument. The first end effector can comprise a first set of stored data pertaining to the first end effector, wherein the surgical instrument is configured to ascertain the first set of data and enter a first operating state. The second end effector can comprise a second set of stored data pertaining to the second end effector, wherein the surgical instrument is configured to ascertain the second set of data and enter a second operating state. The surgical instrument is further configured to enter a default operating state if said surgical instrument is unable to ascertain a set of stored data from an end effector.

Abstract: A surgical instrument includes a shaft, an end effector extending distally from the shaft, and a housing extending proximally from the shaft. The housing includes a motor configured to generate at least one motion to effectuate the end effector, and a power source configured to supply power to the surgical instrument, wherein the power source includes a casing, a data storage unit, and a deactivation mechanism configured to interrupt access to data stored in the data storage unit. In addition, the power source includes a battery pack and a deactivation mechanism configured to deactivate the battery pack if the casing is breached.

Abstract: A surgical instrument includes a shaft, an end effector extending distally from the shaft, and a housing extending proximally from the shaft. The housing includes a motor configured to generate at least one motion to effectuate the end effector, and a power source configured to supply power to the surgical instrument, wherein the power source includes a casing, a data storage unit, and a deactivation mechanism configured to interrupt access to data stored in the data storage unit. In addition, the power source includes a battery pack and a deactivation mechanism configured to deactivate the battery pack if the casing is breached.

Abstract: An apparatus includes a body, a shaft, a stapling head assembly, and an anvil. The body includes a motor, a first user input feature, and a second user input feature. The first user input feature is operable to activate the motor. The shaft extends distally from the body. The stapling head assembly is positioned at a distal end of the shaft. The stapling head assembly includes an anvil coupling feature, at least one annular array of staples, and a staple driver. The second user input feature is operable to drive the anvil coupling feature longitudinally. The staple driver is operable to drive the at least one annular array of staples. The motor is operable to drive the staple driver. The anvil is configured to couple with the anvil coupling feature. The anvil is further configured to deform the staples driven by the staple driver.

Abstract: Circular stapling instruments and anvil assemblies. The anvil assemblies may have collapsible anvil support members that may be inserted through an opening in a patient and then expanded to be attached to an anvil plate assembly that has a staple-forming surface thereon. The anvil support member is attachable to the anvil plate assembly in such a way that when the anvil assembly is coupled to the stapling head of a circular stapler, the staple-forming surface is in substantial registry with the staples supported in the stapling head. A variety of different anvil support members and anvil plate assemblies are disclosed.

Abstract: An apparatus includes a body, a shaft, a stapling head assembly, and an anvil. The body includes a motor, a first user input feature, and a second user input feature. The first user input feature is operable to activate the motor. The shaft extends distally from the body. The stapling head assembly is positioned at a distal end of the shaft. The stapling head assembly includes an anvil coupling feature, at least one annular array of staples, and a staple driver. The second user input feature is operable to drive the anvil coupling feature longitudinally. The staple driver is operable to drive the at least one annular array of staples. The motor is operable to drive the staple driver. The anvil is configured to couple with the anvil coupling feature. The anvil is further configured to deform the staples driven by the staple driver.

Abstract: A compressible adjunct is used with a surgical instrument including a staple cartridge deck. The compressible adjunct includes a first biocompatible material, a second biocompatible material with a lower melting temperature than the first biocompatible material, and a body including a face positionable against a length of the staple cartridge deck. The face includes a plurality of attachment regions spaced apart from one another, wherein the plurality of attachment regions include the second biocompatible material, wherein the face is selectively attachable to the staple cartridge deck at said plurality of attachment regions, and a plurality of non-attachment regions extending between the plurality of attachment regions, wherein the second biocompatible material is selectively disposed outside said non-attachment regions.

Abstract: A packaging assembly is designed for an applicator that contains a buttress assembly that is used with a surgical stapler to reinforce a cut and stapled tissue site. The packaging assembly protects the buttress assembly from damage due to physical contact as well as exposure to adverse environmental factors like excess moisture, etc. In one example the packaging assembly includes a dual tray design with an inner tray that holds the applicator. The combined inner tray and applicator are hermetically sealed within a foil assembly or foil pouch. The foil pouch with the inner tray and applicator within is placed within the outer tray to protect the foil from damage.

Abstract: A surgical system and related methods includes a buttress applier cartridge, a first buttress assembly, and a second buttress assembly. The buttress applier cartridge has a housing and a platform. The first and second buttress assemblies respectively includes first and second buttresses and first and second adhesive layers thereon. The first adhesive layer is parallel to the first buttress and defines a first adhesive pattern having a first outer adhesive profile. The second adhesive layer is parallel to the second buttress and defines a second adhesive pattern having a second outer adhesive profile. The exposed second outer adhesive profile in the transverse direction is the same as the exposed first outer adhesive profile in an opposite transverse direction such that the first and second buttress assemblies are interchangeable with the first and second portions of the end effector of the surgical instrument.

Abstract: A buttress assembly for use with a surgical stapled site has a buttress and an adhesive on one side of the buttress. The adhesive on the buttress is applied in a pattern where the adhesive extends near or along the edges of the buttress while a center region of the buttress remains relatively free of adhesive. The adhesive is applied such that it extends continuously along the buttress and has a height such that the adhesive creates a sealing attachment with an end effector. The adhesive can be applied in an uneven distribution such that there is more adhesive applied at one end of the buttress than the other. The adhesive can also be applied in a symmetric or asymmetric distribution about a longitudinal axis of the buttress.

Abstract: A buttress applier cartridge assembly includes a buttress assembly and a buttress applier cartridge. The buttress assembly includes a buttress configured to support a staple formed therein as well an adhesive layer for adhering to an end effector. The buttress applier cartridge includes a housing defining a gap extending in a longitudinal direction as well as a platform. The platform extends longitudinally from a proximal portion to a distal portion and is exposed in a transverse direction adjacent to the gap. The proximal and distal portions respectively have a proximal stiffness and a different, distal stiffness in the transverse direction. Thereby, the proximal and distal portions support the buttress assembly thereon to deform with the proximal and distal stiffnesses and provide reactionary forces of at least the predetermined minimum force while receiving the end effector for accommodating various camber orientations of the end effector.

Abstract: A method of applying a buttress to a surgically cut and stapled site uses an end effector with a buttress applier cartridge assembly to load one or more buttress assemblies to the end effector. The buttress assemblies each include a buttress to support a staple formed therein as well an adhesive for adhering to the end effector. The adhesive of the buttress assemblies can include a pattern to assist in both attachment to the end effector and release from the end effector after cutting and stapling a tissue site. The buttress applier cartridge can include features that accommodate end effectors having various tip configurations, including straight tips and curved or bent tips.

Abstract: A power system, for powering a surgical instrument including an end effector and a motor configured to generate at least one motion to effectuate the end effector, includes a primary power source configured to supply a first power to operate the surgical instrument, wherein the primary power source is detachable from the surgical instrument, a secondary power source configured to supply a second power to operate the surgical instrument when the primary power source is detached from the surgical instrument, wherein the secondary power source is rechargeable, and wherein the primary power source is configured to charge the secondary power system, and a power management circuit configured to selectively transmit the first power from the primary power source and the secondary power from the secondary power source to operate the surgical instrument.

Abstract: An apparatus includes a housing, a platform, and a buttress assembly. The housing defines a gap configured to receive a portion of an end effector of a surgical stapler. A portion of the platform is exposed in the gap defined by the housing. The buttress assembly is positioned on the platform. The buttress assembly is exposed in the gap defined by the housing. The platform is configured to apply at least two different amounts of pressure against the first buttress assembly in response to a clamping action of an end effector positioned in the gap defined by the housing.

Abstract: A surgical instrument includes a body, a shaft, a cartridge receiving assembly, a suture cartridge, and a slip clutch. The cartridge receiving assembly has a transmission mechanism operatively connected to an actuator of the body. The suture cartridge is received within the cartridge receiving assembly and includes a needle and a drive assembly. The drive assembly is engaged with the transmission mechanism and is coupled with the needle for selectively driving the needle. The slip clutch is operatively connected to the actuator, the transmission mechanism, and the drive assembly such that the slip clutch is configured to transmit a force therethrough from the actuator toward the needle. The slip clutch is configured to slip under the influence of predetermined maximum force transmission therethrough to operatively disengage the needle from the actuator for limiting a driving force applied to the needle.