Some embodiments provide systems, assemblies, and methods of analyzing patient anatomy including providing an analysis of a patient's spine. The systems, assemblies, and/or methods can include obtaining initial patient data, and acquiring spinal alignment contour information. Further, the systems, assemblies, and/or methods can assess localized anatomical features of the patient, and obtain anatomical region data. The system, assemblies, and/or method can analyze the localized anatomy and therapeutic device location and contouring. Further, the system, assemblies, and/or method can output localized anatomical analyses and therapeutic device contouring data and/or imagery on a display.

The invention relates to an optical navigation system for determining the position of a patient's anatomy of interest. The system comprises a locating device having at least two optical sensors and a patient reference having at least three optical markers. The system also comprises a reflecting device. When the line of sight between the patient reference and an optical sensor is intersected by an obstacle, the optical sensors are configured to measure, for each optical marker of the patient reference, a quantity representing the position of said optical marker in the frame of reference of the locating device from optical radiation originating from said optical marker and having a path reflected by the reflecting device to each optical sensor.

An intraluminal sensing device includes a catheter or a guidewire with a flexible elongate member that is positioned within a body lumen of a patient. The device also includes a sensor disposed at a distal portion of the flexible elongate member. The sensor obtains medical data associated with the body lumen while the flexible elongate member is positioned within the body lumen. The sensor is an ultrasound transducer, a pressure sensor, a flow sensor, and/or a temperature sensor. The device further includes a radiopaque marker coupled to the flexible elongate member. The radiopaque marker is an ultraviolet (UV) radiation-cured product of a mixture that includes a radiopaque material, an electromagnetic-radiation-curable adhesive, and a photoinitiator. The solution of the mixture is applied directly to the flexible elongate member and UV radiation-cured to form the radiopaque marker. The radiopaque marker is a band extending around a perimeter of the flexible elongate member.

A system and a method for spatial positioning of magnetometers. Said system includes: magnetometers, a magnetometer support, first positioning markers, a photogrammetry system, and a controller. The first positioning markers are a non-rotationally-symmetrical pattern. The photogrammetry system includes photographing devices configured to photograph, at at least two of a plurality of photographing sites, first image data of the first positioning markers by means of one or more photographing devices. The controller is configured to receive data of the first image photographed by the photographing devices, calculate spatial positions of the first positioning markers on the basis of pre-obtained system parameters and the first image data, and then calculate spatial positions and spatial orientations of the magnetometers.

A patient-specific registration jig for registering an orthopaedic surgical instrument with a bony anatomy of a patient includes a head and an adaptor coupled to the head. The head includes a patient-specific contact surface configured to contact a portion of the patient's bony anatomy such that the head can be coupled to the patient's bony anatomy in a unique position. The adaptor includes an elongated shank having a first end coupled to the head and a second end and an adaptor end attached to the second end of the elongated shank. The adaptor end is configured to be received by a clutch of the orthopaedic surgical instrument. A method for registering the orthopaedic surgical instrument using the patient-specific registration jig is also disclosed.

A retro-reflective marker comprising a bare retro-reflective layer; a protective layer with a near-infrared (NIR) wavelength specific anti-reflective coating; and a border with an NIR absorbent coating.

A presentation device for displaying a graphical presentation of an augmented reality is disclosed. The presentation device includes a recording unit, a first display unit, and a processing unit. The recording unit is configured to capture a relative positioning of the first display unit in respect of a presentation area and capture a second set of graphical information. The processing unit is configured to generate an augmented reality based on a received dataset, supply a graphical presentation of the augmented reality by virtual mapping to the presentation area, and adjust the augmented reality and/or the graphical presentation thereof as a function of the second set of graphical information. The first display unit is at least partially transparent and is configured to display the graphical presentation of the augmented reality.

A number of improvements are provided relating to computer aided surgery utilizing an on tool tracking system. The various improvements relate generally to both the methods used during computer aided surgery and the devices used during such procedures. Other improvements relate to the structure of the tools used during a procedure and how the tools can be controlled using the OTT device. Still other improvements relate to methods of providing feedback during a procedure to improve either the efficiency or quality, or both, for a procedure including the rate of and type of data processed depending upon a CAS mode.

A biopsy device includes a cannula and a specimen collector. The cannula has a proximal end and a longitudinal axis. The specimen collector contains the proximal end of the cannula. The specimen collector has a removable sample receiving cartridge that is removable along the longitudinal axis of the cannula to expose the proximal end of the cannula.

The disclosure is directed to an implant tool and cannula used to facilitate the implantation of a medical device into a patient. The implant tool includes a housing that is held by a user and a needle attached to the housing. The cannula may be positioned over the needle and delivered to a target tissue within the patient. The cannula includes an electrode at a distal portion to deliver test stimulation to confirm the location of the target site or placement of the implant tool relative to the target site before removing the needle of the implant tool. In this manner, the cannula may be repositioned within the patient until the position of the implant tool and cannula relative to the target site is verified with the test stimulation.