K Number
K962315

Validate with FDA (Live)

Date Cleared
1996-09-03

(78 days)

Product Code
Regulation Number
888.3650
Age Range
All
Reference & Predicate Devices
N/A
Predicate For
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

Not Found

Device Description

The Select Shoulder Humeral Stem is a metallic humeral component manufactured from cobalt chrome alloy (CoCrMo) and is intended for use with bone cement in total shoulder arthroplasty. The humeral stem is available in a variety of sizes and features a proximally grit blasted surface (except for the head stem taper) for enhanced cement fixation. The proximal trapezoidal shape tapers in the A-P plane, thus providing for a stable cement mande. The proximal body also features an antirotation fin on the lateral aspect. Suture holes are provided in the medial proximal body and lateral fin to allow for soft tissue/bony fragment attachment and tensioning, thus resulting in a more biomechanically stable construct for repair for proximal fractures. A male IOI morse type taper permits attachment of one of the metallic humeral heads offered by Intermedics Orthopedics. This taper is identical to the taper of the previously cleared Select Shoulder System. Distally, the stem is rounded and fluted to provide enhanced fixation and rotational stability. The distal stem tip is designed to accept a cement centralizer. The humeral stem is designed for use with Intermedics Orthopedics humeral heads and glenoid components in a variety of sizes and heights for increased stability of the glenohumeral joint.

AI/ML Overview

This document is a 510(k) summary for a medical device (Intermedics Orthopedics, Inc. Select® Shoulder System CoCr Humeral Stem) and describes its physical characteristics and intended use. It does not contain any information about acceptance criteria or a study proving the device meets acceptance criteria related to AI/ML performance.

Therefore, I cannot fulfill your request for information regarding:

  1. A table of acceptance criteria and the reported device performance
  2. Sample size used for the test set and the data provenance
  3. Number of experts used to establish the ground truth for the test set and their qualifications
  4. Adjudication method
  5. Multi-reader multi-case (MRMC) comparative effectiveness study
  6. Standalone performance
  7. Type of ground truth used
  8. Sample size for the training set
  9. How the ground truth for the training set was established

The provided text focuses on the mechanical and material properties of a humeral stem and its equivalence to other legally marketed devices, rather than on the performance of an AI/ML algorithm.

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3 SEP

K962315

510(k) SUMMARY

June 6, 1996

In accordance with the Food and Drug Administration Interim Rule to implement provisions of the Safe Medical Devices Act of 1990 and in conformance with 21CFR 807, this is to serve as a 510(k) Summary for the Intermedics Orthopedics, Inc. Select® Shoulder System CoCr Humeral Stem.

Submitter:Intermedics Orthopedics, Inc.9900 Spectrum DriveAustin, TX 78717(512) 432-9900
Contact Person:Jacquelyn HughesManager, Regulatory Affairs
Classification Name:Shoulder joint metal/polymer non-constrained cementedprosthesis - 21 CFR Part 888.3650
Shoulder joint metal/polymer semi-constrained cementedprosthesis - 21 CFR Part 888.3660
Common/Usual Name:Humeral Stem
Trade/Proprietary:Select® Shoulder CoCr Humeral Stem

Product Description/Substantial Equivalence:

The Select Shoulder Humeral Stem is a metallic humeral component manufactured from cobalt chrome alloy (CoCrMo) and is intended for use with bone cement in total shoulder arthroplasty. The humeral stem is available in a variety of sizes and features a proximally grit blasted surface (except for the head stem taper) for enhanced cement fixation. The proximal trapezoidal shape tapers in the A-P plane, thus providing for a stable cement mande. The proximal body also features an antirotation fin on the lateral aspect. Suture holes are provided in the medial proximal body and lateral fin to allow for soft tissue/bony fragment attachment and tensioning, thus resulting in a more biomechanically stable construct for repair for proximal fractures. A male IOI morse type taper permits attachment of one of the metallic humeral heads offered by Intermedics Orthopedics. This taper is identical to the taper of the previously cleared Select Shoulder System. Distally, the stem is rounded and fluted to provide enhanced fixation and rotational stability. The distal stem tip is designed to accept a cement centralizer. The humeral stem is designed for use with Intermedics Orthopedics humeral heads and glenoid components in a variety of sizes and heights for increased stability of the glenohumeral joint.

Fatigue analysis and taper testing of the Select Shoulder Humeral Stem indicated that the device would survive physiologic loading.

The Select Shoulder CoCr Humeral Stem is similar to those of the Depuy Global Total Shoulder System, the Biomet Bio-Modular Total Shoulder, the Zimmer Fenlin Total Shoulder, the Kirschner Integrated Shoulder System, the 3M/Orthomet Neer II Shoulder System, and the Smith

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& Nephew Richards Cofield Shoulder.

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000337

N/A