Abstract:
A tissue anchor system includes a support material, a suture engaged with the support material, an anchor, and an introducer. The anchor has a body, a fin extending from the body in a first direction with an eyelet formed in the fin, a pair of radial barrels extending from the body in a radial direction perpendicular to the first direction, and a gripping tab removably attached to the fin. The suture is engaged with the eyelet of the fin. The introducer has a cannula with a bore sized to receive the body of the anchor and a slot formed in a wall of the cannula. The slot is sized to receive the fin of the anchor, and an ejection mechanism provided to eject the anchor out of the cannula.
Abstract:
A method of fixating an implantable material in a patient includes forming an incision in the patient. The method includes inserting an anchor into a bore of a cannula, with the anchor attached to a support by a suture that is looped through an eyelet of the anchor and engaged through the support. The method includes inserting the cannula into the incision and along a cannula path into soft tissue, and ejecting the anchor out of the bore of the cannula and into the soft tissue. The suture is pulled in a direction away from the patient, moving the anchor to position a length of the anchor transverse to the cannula path. The method includes tying a knot in the suture, driving the knot against the support, and fixating the support in the patient.
Abstract:
A tissue anchor has a body, protrusions from the body, and a tissue engaging fin. The body is oriented on a longitudinal axis and has a leading tip, a leading end portion extending from the leading tip, a trailing end portion connected to the leading end portion, with the trailing end portion terminating in a trailing tip that is located opposite of the leading tip. A first anchor width measured between the protrusions is greater than a second anchor width measured at the trailing end portion of the body. The tissue engaging fin is integrated with the leading end portion of the body and oriented in a direction perpendicular to the radial direction of the first and second protrusions. The tissue engaging fin has a fin width and is provided with an eyelet formed through the fin width. A gripping tab is removably attached to the tissue engaging fin.
Abstract:
An end effector is disclosed which comprises a first jaw, a second jaw, a staple cartridge, an anvil, and at least one layer positioned intermediate the first jaw and the second jaw. The layer may include a pattern of holding features defined on a tissue contacting surface of the layer. The pattern of holding features can extend between a proximal end of the layer and a distal end of the layer. The pattern of holding features may be defined by a network of interconnected channels skew to a longitudinal axis of the layer. The network of interconnected channels may be configured to mitigate and/or control the flow of patient tissue relative to the layer.
Abstract:
A tissue thickness compensator can comprise a tissue contacting surface and a network of channels defined in the tissue contacting surface. In at least one embodiment, the channels can be configured to store at least one medicament therein. In certain embodiments, the channels can define gripping surfaces configured to grip tissue. In various embodiments, the tissue contacting surface can further comprise ridges extending therefrom.
Abstract:
Devices, methods and systems are provided for occluding an opening within the tissue of a body, such as a left atrial appendage. In one embodiment, a delivery system for use in occluding an opening in the tissue of a body includes an actuation assembly operatively coupled to a medical device including an anchor portion and an occluder portion. The actuation assembly is configured to move the anchor portion between a deployed state and retracted state while the occluder portion maintains a deployed state. With this arrangement, the deployed occluder portion can be visualized via imaging at a preferred position prior to deploying the anchor portion of the medical device.
Abstract:
A staple cartridge assembly for use with a surgical stapler. The assembly has a cartridge body having a support portion with a plurality of staple cavities with openings. There is also a plurality of staples, wherein at least a portion of each the staple is removably stored within the staple cavity. Each the staple is movable between an unfired position and a fired position, and is deformable between an unfired configuration and a fired configuration. The assembly also includes a compressible tissue thickness compensator configured to be captured within the staples. The compressible tissue thickness compensator at least partially covers the staple cavity openings. The compressed tissue thickness compensator is configured to assume different compressed heights within different the staples. The compressible tissue thickness compensator comprising a lyophilized foam having a hemostatic agent embedded therein.
Abstract:
A tissue thickness compensator may generally comprise a first layer comprising a first medicament, a second layer comprising a second medicament, and a third layer comprising a third medicament. The tissue thickness compensator may comprise a first layer comprising a first medicament, a second layer comprising a second medicament, and a reservoir comprising a third medicament disposed within the reservoir. The medicaments may be independently selected from a haemostatic agent, an anti-inflammatory agent, an antibiotic agent, anti-microbial agent, an anti-adhesion agent, an anti-coagulant agent, a pharmaceutically active agent, a matrix metalloproteinase inhibitor, and combinations thereof. Articles of manufacture comprising the tissue thickness compensator and methods of making and using the tissue thickness compensator are also described.
Abstract:
A staple cartridge assembly for use with a surgical stapler. The assembly has a cartridge body having a support portion with a plurality of staple cavities with openings. There is also a plurality of staples, wherein at least a portion of each the staple is removably stored within a the staple cavity. Each the staple is movable between an unfired position and a fired position, and is deformable between an unfired configuration and a fired configuration. The assembly also includes a compressible tissue thickness compensator configured to be captured within the staples. The compressible tissue thickness compensator at least partially covers the staple cavity openings. The compressed tissue thickness compensator is configured to assume different compressed heights within different the staples. The compressible tissue thickness compensator comprising a lyophilized foam having an oxygen generating agent embedded therein.
Abstract:
A tissue thickness compensator can comprise a plurality of layers. Various embodiments are disclosed herein for manufacturing a tissue thickness compensator. In certain embodiments, a tissue thickness compensator can comprise at least one medicament tube, capsule, and/or packet contained therein.