FDA 510(k)

ARTHREX UNIVERS II SHOULDER PROSTHESIS

K-Number: K103466 · 2010-12-22

Decision Date2010-12-22

Product CodeKWS

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

ARTHREX UNIVERS II SHOULDER PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2010-12-22 under 510(k) number K103466. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHREX UNIVERS II SHOULDER PROSTHESIS?

ARTHREX UNIVERS II SHOULDER PROSTHESIS is a medical device that received FDA 510(k) clearance on 2010-12-22. The listed applicant is Arthrex, Inc.. The 510(k) number is K103466.

When did ARTHREX UNIVERS II SHOULDER PROSTHESIS receive FDA 510(k) clearance?

ARTHREX UNIVERS II SHOULDER PROSTHESIS received FDA 510(k) clearance on 2010-12-22, under 510(k) number K103466.

Who is the listed applicant for ARTHREX UNIVERS II SHOULDER PROSTHESIS?

The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHREX UNIVERS II SHOULDER PROSTHESIS?

The FDA product code for ARTHREX UNIVERS II SHOULDER PROSTHESIS is KWS.

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Related Devices (Code: KWS)

K260721Tornier Perform Advanced GlenoidTornier, Inc.K254084AETOS Shoulder System - CONCELOC GlenoidsSmith & Nephew, Inc.K252418Catalyst F1x Shoulder SystemCatalyst Orthoscience, Inc.K252416AETOS Shoulder System Meta Humeral Prosthesis Size 0Smith & Nephew, Inc.K241292MyShoulder Planner (5.3SSWPL)Medacta International S.A.K241878Tornier Humeral Reconstruction System (Tornier HRS); Tornier Perform Humeral System - Stem (Tornier PHS-Stem)Stryker Corporation (Tornier, Inc.)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.