Surgical Instrument Handle With Implant Sizing Feature and Method of Using

20190298322 ยท 2019-10-03

Assignee

Inventors

Cpc classification

International classification

Abstract

A single-use handle for releasably engaging an orthopedic device, said handle comprising: an elongate body, said body having a first portion defining a connection end adapted for connection to the upper end portion of the broach, and a second portion adapted to be gripped by a user; said body further comprising a longitudinal axis, and a cylindrical bore disposed along said longitudinal axis in communication with said connection end; said bore adapted to receive a corresponding male portion of a surgical instrument; a button, said button disposed on the exterior of said body and adapted to selectively and means for releasably connecting said instrument to said bore; a plurality of spherical cavities disposed on the exterior of said body, each cavity of said plurality of cavities having a predetermined size and shape where said shape corresponds to the size and shape of an orthopedic implant, said handle comprising a biocompatible, disposable, material.

Claims

1. A single-use handle for releasably engaging an orthopedic device, said handle comprising: an elongate body, said body having a first portion defining a connection end adapted for connection to the upper end portion of the broach, and a second portion adapted to be gripped by a user; said body further comprising a longitudinal axis, and a cylindrical bore disposed along said longitudinal axis in communication with said connection end; said bore adapted to receive a corresponding male portion of a surgical instrument; a button, said button disposed on the exterior of said body and adapted to selectively and means for releasably connecting said instrument to said bore; a plurality of spherical cavities disposed on the exterior of said body, each cavity of said plurality of cavities having a predetermined size and shape where said shape corresponds to the size and shape of an orthopedic implant, said handle comprising a biocompatible, disposable, material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0011] The present invention will be understood more fully from the detailed description given hereinafter and from the accompanying drawings of the preferred embodiment of the present invention, which, however, should not be taken to limit the invention, but are for explanation and understanding only.

[0012] In the drawings:

[0013] FIG. 1 shows prior art sizing devices.

[0014] FIG. 2 shows a top view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0015] FIG. 3 shows a bottom view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0016] FIG. 4 shows a first end view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0017] FIG. 5 shows a second end view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0018] FIG. 6 shows a side view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0019] FIG. 7 shows a side view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0020] FIG. 8 shows a view of an apparatus in accordance with an exemplary embodiment of the present invention.

[0021] Corresponding reference characters indicate corresponding parts throughout the several views. The exemplary embodiments set forth herein are not to be construed as limiting the scope of the invention in any manner.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0022] The present invention will be discussed hereinafter in detail in terms of various exemplary embodiments according to the present invention with reference to the accompanying drawings. In the following detailed description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. It will be obvious, however, to those skilled in the art that the present invention may be practiced without these specific details. In other instances, well-known structures are not shown in detail in order to avoid unnecessary obscuring of the present invention.

[0023] Thus, all of the implementations described below are exemplary implementations provided to enable persons skilled in the art to make or use the embodiments of the disclosure and are not intended to limit the scope of the disclosure, which is defined by the claims. As used herein, the word exemplary or illustrative means serving as an example, instance, or illustration. Any implementation described herein as exemplary or illustrative is not necessarily to be construed as preferred or advantageous over other implementations. Moreover, in the present description, the terms upper, lower, left, rear, right, front, vertical, horizontal, and derivatives thereof shall relate to the invention as oriented in FIG. 1.

[0024] Furthermore, there is no intention to be bound by any expressed or implied theory presented in the preceding technical field, background, brief summary or the following detailed description. It is also to be understood that the specific devices and processes illustrated in the attached drawings, and described in the following specification, are simply exemplary embodiments of the inventive concepts defined in the appended claims. Hence, specific dimensions and other physical characteristics relating to the embodiments disclosed herein are not to be considered as limiting, unless the claims expressly state otherwise.

[0025] Referring now to FIGS. 1-3, there are shown various prior art radial head sizing devices. In current surgical techniques for radial head replacement, surgeons typically use the following steps: (1) performing an initial skin incision; (2) performing an extensor split; (3) resecting the radial neck; (4) reaming the canal; (5) planing the resected surface; (6) rebuilding the fragments in a sizer dish; (6) assembling the trial implant; (7) inserting the trial implant; (8) performing a trial range of motion; (9) removing the trial implant; (10) disassembling and reassembling the trial implant; (11) inserting the trial implant; (12) performing another trial range of motion; (13) removing the trial implant; and (14) inserting the final implant.

[0026] Those of skill in the art will appreciate that prior art devices require various instrument sets to remove and reassemble the trial implant. Additionally, a surgeon must use a remote sizing device to determine the appropriate radial head implant size.

[0027] Referring now to FIGS. 4 and 5, which show, respectively, a top view and a bottom view of handle 1000 in accordance with an exemplary embodiment of the present invention. As illustrated in FIG. 4, handle 1000 comprises an elongate, preferably tapered, body. Handle 1000 further comprises a plurality, preferably at least three, sizing cavities 100. It is preferred to have three or more cavities to reduce the likelihood that a surgeon will have to use a separate device to size the humeral head.

[0028] Referring still to FIGS. 4-5 as well as to FIG. 7, where there is shown a side view of apparatus 1000, each cavity 100 comprises a unique size and my also comprise a unique shape. However, in the preferred embodiment, each cavity 100 is generally spherical in shape.

[0029] Referring now to FIGS. 6-7, FIG. 6 shows proximal end 110 of handle 1000. FIG. 7 shows opposing distal connecting end 120 of handle 100. Handle 100, in one exemplary embodiment, comprises a channel 130 along the longitudinal axis (not shown) of handle 1000 for releasably receiving a corresponding male portion of a surgical device. As shown in FIG. 4, handle 100 may comprise a button 140 other quick release mechanism for engaging such male shaft of a surgical instrument.

[0030] Handle 100 comprises biocompatible, disposable materials. Preferably, handle 100 comprises biocompatible, disposable, recyclable materials.

[0031] While this invention has been described with respect to at least one embodiment, the present invention can be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fall within the limits of the appended claims.