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FDA 510(k)

PARTNERSHIP REVISION FEMORAL STEMS

K-Number: K972893 · 1997-11-03

ApplicantHowmedica Corp.
Decision Date1997-11-03
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PARTNERSHIP REVISION FEMORAL STEMS is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1997-11-03 under 510(k) number K972893. 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 PARTNERSHIP REVISION FEMORAL STEMS?

PARTNERSHIP REVISION FEMORAL STEMS is a medical device that received FDA 510(k) clearance on 1997-11-03. The listed applicant is Howmedica Corp.. The 510(k) number is K972893.

When did PARTNERSHIP REVISION FEMORAL STEMS receive FDA 510(k) clearance?

PARTNERSHIP REVISION FEMORAL STEMS received FDA 510(k) clearance on 1997-11-03, under 510(k) number K972893.

Who is the listed applicant for PARTNERSHIP REVISION FEMORAL STEMS?

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

What is the FDA product code for PARTNERSHIP REVISION FEMORAL STEMS?

The FDA product code for PARTNERSHIP REVISION FEMORAL STEMS is LZO.

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Other records listing Howmedica Corp. as applicant

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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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Related Devices (Code: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 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.

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