FDA 510(k)

SOLUTION BOWED FEMORAL HIP PROTSTHESIS

K-Number: K933942 · 1994-10-14

Decision Date1994-10-14

Product CodeLZO

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SOLUTION BOWED FEMORAL HIP PROTSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1994-10-14 under 510(k) number K933942. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLUTION BOWED FEMORAL HIP PROTSTHESIS?

SOLUTION BOWED FEMORAL HIP PROTSTHESIS is a medical device that received FDA 510(k) clearance on 1994-10-14. The listed applicant is Depuy, Inc.. The 510(k) number is K933942.

When did SOLUTION BOWED FEMORAL HIP PROTSTHESIS receive FDA 510(k) clearance?

SOLUTION BOWED FEMORAL HIP PROTSTHESIS received FDA 510(k) clearance on 1994-10-14, under 510(k) number K933942.

Who is the listed applicant for SOLUTION BOWED FEMORAL HIP PROTSTHESIS?

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

What is the FDA product code for SOLUTION BOWED FEMORAL HIP PROTSTHESIS?

The FDA product code for SOLUTION BOWED FEMORAL HIP PROTSTHESIS is LZO.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: LZO)

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic Corporation K261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KG K260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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.