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FDA 510(k)

Arthrex Shoulder System

K-Number: K171841 · 2018-03-29

ApplicantArthrex, Inc.
Decision Date2018-03-29
Product CodeKWS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Arthrex Shoulder System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2018-03-29 under 510(k) number K171841. 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 Shoulder System?

Arthrex Shoulder System is a medical device that received FDA 510(k) clearance on 2018-03-29. The listed applicant is Arthrex, Inc.. The 510(k) number is K171841.

When did Arthrex Shoulder System receive FDA 510(k) clearance?

Arthrex Shoulder System received FDA 510(k) clearance on 2018-03-29, under 510(k) number K171841.

Who is the listed applicant for Arthrex Shoulder System?

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 Shoulder System?

The FDA product code for Arthrex Shoulder System is KWS.

Other records listing Arthrex, Inc. as applicant

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Related Devices (Code: KWS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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