Embodiments of the invention are directed towards a medical device, method and system thereof for the placement or passage of patches, sutures, anchors, tags, tissue sensors and more particularly to a medical device for repairing female pelvic organ or tissue prolapsed region. The device may be used for the placement of stereotactic markers into tissue near joints or tumors for guidance during orthopedic or neurosurgical procedures.

Embodiments of the invention are directed towards a medical device, method and system thereof for the placement or passage of patches, sutures, anchors, tags, tissue sensors and more particularly to a medical device for repairing female pelvic organ or tissue prolapsed region. The device may be used for the placement of stereotactic markers into tissue near joints or tumors for guidance during orthopedic or neurosurgical procedures.

A surgical access assembly includes a sleeve assembly, a base member, and a sealing assembly. The sleeve assembly includes a proximal ring, a distal ring, and a sleeve defining a passage therethrough. The base member includes an annular body including a coupling member. The annular body defines an opening in communication with the passage of the sleeve, and a circumferential groove configured to support the proximal ring of the sleeve assembly. The sealing assembly includes an annular frame and a seal dimensioned to cover the opening of the base member in a sealing relation. The coupling member of the base member releasably secures the sealing assembly to the base member. The annular frame of the sealing assembly is configured to be in registration with the annular body of the base member such that the proximal ring is interposed between the base member and the sealing assembly.

A surgical access sealing device comprises expansile chambers 306, 307, 308, 309 which define inflation spaces. An upper layer 304 in one case comprises two chambers 306, 307 which are overlapped when uninflated. A lower layer 305 comprises two chambers 308, 309 which are also overlapped, when uninflated. The region of overlap between the chambers 306, 307 of the first layer is offset from the region of overlap between the chambers 308, 309 of the second layer. The walls of the inflated chambers are movable for passage of an object such as a surgeon's arm/hand whilst maintaining a seal.

A surgical access assembly includes a sleeve assembly, a base member, and a sealing assembly. The sleeve assembly includes a proximal ring, a distal ring, and a sleeve defining a passage therethrough. The base member includes an annular body including a coupling member. The annular body defines an opening in communication with the passage of the sleeve, and a circumferential groove configured to support the proximal ring of the sleeve assembly. The sealing assembly includes an annular frame and a seal dimensioned to cover the opening of the base member in a sealing relation. The coupling member of the base member releasably secures the sealing assembly to the base member. The annular frame of the sealing assembly is configured to be in registration with the annular body of the base member such that the proximal ring is interposed between the base member and the sealing assembly.

A surgical access assembly includes a sleeve assembly, a base member, and a sealing assembly. The sleeve assembly includes a proximal ring, a distal ring, and a sleeve defining a passage therethrough. The base member includes an annular body including a coupling member. The annular body defines an opening in communication with the passage of the sleeve, and a circumferential groove configured to support the proximal ring of the sleeve assembly. The sealing assembly includes an annular frame and a seal dimensioned to cover the opening of the base member in a sealing relation. The coupling member of the base member releasably secures the sealing assembly to the base member. The annular frame of the sealing assembly is configured to be in registration with the annular body of the base member such that the proximal ring is interposed between the base member and the sealing assembly.

A system for controlling displacement of an intervention device having an end for inserting in a patient body, including a base in a fixed position relative to the patient. A first portion has an arc member and is pivotally mounted on the base around a first axis (A1). A second portion includes a support member and a carrier member. The support member partially rotates around a second axis (A2). A third portion includes a holding member, and a sliding member mounted on the support member along a translation axis (A.sub.T). The holding member is arranged so that translation of the sliding member causes the intervention device to translate along a third axis (A3). The third axis (A3) is parallel to and offset from the translation axis (A.sub.T). When the carrier member is positioned halfway of the arc member, the first (A1), second (A2) and third (A3) axes are orthogonal.

Devices, methods, and systems provide a surgical access device comprising an internal retractor device integrated with or coupled to a body wall or wound retractor. The wound retractor retracts an opening in a body wall into a body cavity, while the internal retractor permits a user to control the positions of internal structures within the body cavity, thereby permitting a user to define a surgical field. Embodiments of the internal retractor are adjustable.

Embodiments of the invention are directed towards a medical device, method and system thereof for the placement or passage of patches, sutures, anchors, tags, tissue sensors and more particularly to a medical device for repairing female pelvic organ or tissue prolapsed region. The device may be used for the placement of stereotactic markers into tissue near joints or tumors for guidance during orthopedic or neurosurgical procedures.

A surgical access attachment for use with a surgical access device is disclosed. The surgical access attachment includes a ring and an access portion assembly. The ring is configured to engage a proximal portion of a surgical access device. The access portion assembly includes at least one flexible tab having an engagement structure. The engagement structure is configured to selectively engage the ring. The access portion assembly is configured to retain a seal. The access portion assembly is configured to disengage from the ring in response to a predetermined amount of force exerted on one flexible tab of the at least one flexible tab.