FDA 510(k)

SMITH & NEPHEW HIP SYSTEM

K-Number: K022902 · 2002-10-02

Decision Date2002-10-02

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SMITH & NEPHEW HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2002-10-02 under 510(k) number K022902. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMITH & NEPHEW HIP SYSTEM?

SMITH & NEPHEW HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2002-10-02. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K022902.

When did SMITH & NEPHEW HIP SYSTEM receive FDA 510(k) clearance?

SMITH & NEPHEW HIP SYSTEM received FDA 510(k) clearance on 2002-10-02, under 510(k) number K022902.

Who is the listed applicant for SMITH & NEPHEW HIP SYSTEM?

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

What is the FDA product code for SMITH & NEPHEW HIP SYSTEM?

The FDA product code for SMITH & NEPHEW HIP SYSTEM is LPH.

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K261453G7® Acetabular SystemZimmer Biomet K253630Mpact 3D Metal FoamMedacta International S.A.K254043TRIVANCE™ Hip StemGlobus Medical, Inc.K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar ComponentHowmedica Osteonics Corp., Dba Stryker Orthopaedics K243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLC K251270Taperloc® Complete Hip StemBiomet, Inc.

Official Source

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