A system for introducing a surgical instrument through a tissue lumen having: a surgical instrument; a dilator for dilating bodily tissue having an elongated body for positioning the dilator and a tapered section for facilitating dilation of the tissue lumen; and a cone having conical body that tapers from the proximal end to the distal end and facilitates insertion of the cone and the surgical instrument through the tissue lumen, an axial bore that extends longitudinally through the cone and receives an anvil retainer, a collar that engages the distal end of the surgical device and prevents lateral movement of the cone, grooves that engage the surface of the tapered section and reduce the friction between the cone and the tissue lumen, a securing device for securing the cone to the surgical instrument, and a retrieval device for retrieving the cone from a bodily cavity.

Various stabilizers for supporting a trocar and stylet are disclosed. In some implementations, a stabilizer may include a main portion through which a trocar and stylet may be inserted and supported, and a plurality of stabilizing portions to prevent movement of the stabilizer when the stabilizer is placed on a patient's body.

A template grid which attaches to an ultrasound stepper of a transrectal ultrasound unit providing transperineal guidance and support through adjustable angle apertures allowing for accurate targeting of a medical implant such as a needle to its intended target such as for purposes of perirectal spacer placement. The rotational apertures allow for free adjustable changes in the trajectory of a medial implant such as a needle to its intended target while providing stability and support to the medical implant itself. The template grid, in addition, contains fixed apertures for placement of a medical implant such as a needle into the substance of the prostate gland positioned to avoid inadvertent passage through the urethra and rectum.

A puncture adapter of an embodiment holds a puncture needle and is attached to an ultrasonic probe having an ultrasonic probe group. The puncture adapter has a puncture bracket that can be fixed to the ultrasonic probe and a puncture needle guide that is attached to the puncture bracket. The puncture bracket is not fixed to the ultrasonic probe when the puncture needle guide is not attached. The puncture bracket is fixed to the ultrasonic probe when the puncture needle guide is attached.

Systems, devices, and methods for performing Lapidus bunionectomy procedures are disclosed. An example method includes inserting a plurality of metatarsal pins into the first metatarsal at a first predetermined spacing relative to the first tarsometatarsal (TMT) joint, excising the first TMT joint by cutting the bases of the first metatarsal and the first cuneiform proximate the first TMT joint, inserting a plurality of cuneiform pins into the first cuneiform at a second predetermined spacing relative to the first TMT joint, compressing the first TMT joint using a compressor block such that a cut face of the first metatarsal contacts a cut face of the first cuneiform, and fixing the first TMT joint using a bone plate and a plurality of bone screws. At least one of the plurality of bone screws may be a cross screw extending at an angle of less than 90 degrees relative to the bone plate and may anchor the resected first TMT joint to the second metatarsal or the second cuneiform to prevent recurrence of the bunion.

An apparatus for controlling a needle guide includes a first lever, a second lever, a first cam and a second cam. The first cam is attached to and extends from the first lever to a housing under the needle guide. The second cam is attached to and extends from the second lever to the housing under the needle guide. At least one of the first cam and the second cam is configured to translate rotational movement from the first lever and the second lever to both linear and rotational movement of the needle guide via the housing.

A needle having a first end, a second end, and a lumen extending within an interior of the needle, between the first end and the second end. A sleeve is engageable within an interior diameter or interior surface of the lumen. The sleeve includes a first end and a second end that are sized to reside within the first end of the lumen and the second end of the lumen, respectively. Ports extend between the first end and the second end of the sleeve. The ports have an inlet and an outlet sized to receive and route stimulator wires to areas within the epidural space of a spine.

The invention refers to an apparatus allowing to determine a planned position of a temperature probe during a planning for an ablation procedure. The apparatus comprises an ablation plan providing unit (121) for providing an ablation plan, wherein the ablation plan comprises geometric information of an ablation region and of a protection region. The protection region should be protected from ablation. The geometric information comprises information on a position and shape of a respective region. A temperature probe position determination unit (122) is adapted to determine a planned position of the temperature probe, wherein the planned position of the temperature probe is determined based on the geometric information of the ablation region and of the protection region. The apparatus allows to increase the protection of regions that should be protected, like a specific organ, such that the security of an ablation procedure for a patient can also be increased.

The present disclosure includes customized guidance devices in the form of guidance templates configured to fit over a given area of a patient's body and provide guidance during a tissue treatment or tissue removal procedure of that given area, which may include administration of an agent to a target tissue, target tissue biopsy, target tissue resection, or target tissue ablation. The customized guidance templates are generally constructed via an additive manufacturing process (i.e., three-dimensional (3D) printing) or subtractive manufacturing process (i.e., milling) based on a fabrication instruction file, which may include imaging data of the given area of the patient's body in which targeted tissue treatment is to be performed. The fabrication instruction file may further include additional data, such as the type of procedure to be performed (i.e., biopsy of the tissue abnormality, destruction or resection of the tissue abnormality, etc.).

A system for treating obstructive sleep apnea (OSA) is described. The system may include a device having a size and shape selected to couple externally to a patient near a jaw of the patient. The device may be configured to receive at least one of a needle or an introducer for insertion into a tongue of the patient for lead placement of a lead for OSA treatment, and guide at least a portion of the at least one of the needle or introducer for insertion into the tongue of the patient.