A interconnectable port is provided. The interconnectable port is adapted to be at least partially placed in an incision in a patient's body. The interconnectable port comprises a first and second port adapted be interconnected to form the interconnectable port, wherein the second port is disconnectable from the first port, wherein the first port is connected to a first portion of a flexible wall, and the second port is connected to a second portion of the flexible wall, and wherein the flexible wall is adapted to form a chamber.

A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective barrier from contamination.

A device is provided for enclosing an extremity of a patient for container efficient wound cleaning and for integrating draping prior to surgery. A loose-fitting flexible container with a flexible seal is provided for enclosing the extremity and treating the extremity in a controlled fashion to reduce or eliminate spillage and unwanted dispersion of antiseptic solution. Sealed to the flexible container is a vacuum packed, folded and rolled sterile surgical drape. The combination of a flexible container and a sterile pre-positioned surgical drape in a single device provides the advantage of controlled decontamination of the skin or wound while simultaneously providing the advantage of pre-positioning a surgical drape. The use of the device also provides the advantages of reduced operating room fires and biohazard dispersion risk and reduced cost by reduction of total operating room time per procedure.

A disposable, multiple layer surgical drape is provided. The surgical drape includes a bottom layer configured as a fluid impervious layer, a middle layer configured as a fluid absorbent layer, and a top layer configured as a fluid repellent layer. The middle layer is disposed between the top and bottom layers and has varying thickness. The top layer includes one or more continuity breaks exposing the middle layer.

A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective harder from contamination.

A disposable, multiple layer surgical drape is provided. The surgical drape includes a bottom layer configured as a fluid impervious layer, a middle layer configured as a fluid absorbent layer, and a top layer configured as a fluid repellent layer. The middle layer is disposed between the top and bottom layers and has varying thickness. The top layer includes one or more continuity breaks exposing the middle layer.

A method for placing an implant on a patient in a robotic surgical procedure using a robotic system. During the robotic surgical procedure, a navigation system tracks the patient. The navigation system also provides information to the robotic system to guide movement of a cutting tool to remove material from the patient such that a cut surface is created to receive the implant. The implant is then robotically placed on the cut surface.

A medical drape (100) includes an upper portion (101) and a lower portion (102). The upper portion (101) can be pellucid, while the lower portion (102) can be opaque. To facilitate central catheter insertion, the upper portion (101) can define one or more apertures (104,105) through which a central line may be inserted. A tourniquet (401) may be integrated with the drape, as can one or more tool-less removal features (108,109).

An apparatus for supporting an extremity during tissue irrigation and debridement and containing and capturing fluid and tissue debris resulting therefrom includes an extremity-supporting base and barrier shroud. The apparatus can be used to control drainage of fluid and tissue debris during irrigation and debridement. The apparatus supports and encloses a patient extremity, such as an arm or a leg. The base has a length, proximal end (i.e., nearest the patient's body), and distal end (i.e., farthest from the patient's body). The base may comprise an open-cell foam that is non-collapsible to provide a support surface with a fixed length. The shroud has a top portion, bottom portion, and shroud drainage opening. The shroud can be selectively moveable between a first position in which the support surface is unobstructed to facilitate placement of an extremity thereon and a second position in the shroud at least partially encloses the extremity.

A sterile femoral drape intended to be placed over a surgical patient lying on an operating table to isolate the patient during the surgical procedure, the drape comprising a top sheet of bio-impermeable material of a length and width greater than a conventional operating table such that the top sheet fully encompasses the patient and drapes over the lateral side edges and the bottom (foot) edge of the table. Femoral access holes located proximate to the patient's groin are provided to allow access to the patient's femoral artery during heart catheterizations or other surgical procedures. The drape comprises left and right arm pockets formed underneath the bio-impermeable sheet into which the patient's respective left and right arms are inserted. The patient's arms being positioned within and supported within the arm pockets, fully isolates the patient's arms and hands from the femoral access site, thereby assuring that the patient's hands do not contaminate the femoral access site.