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FDA 510(k)

KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL

K-Number: K920290 · 1992-11-03

ApplicantKinamed, Inc.
Decision Date1992-11-03
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 1992-11-03 under 510(k) number K920290. 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 KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL?

KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL is a medical device that received FDA 510(k) clearance on 1992-11-03. The listed applicant is Kinamed, Inc.. The 510(k) number is K920290.

When did KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL receive FDA 510(k) clearance?

KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL received FDA 510(k) clearance on 1992-11-03, under 510(k) number K920290.

Who is the listed applicant for KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL?

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

What is the FDA product code for KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL?

The FDA product code for KINAMED 32MM BIOCERAM-Z TOATAL HIP FEMORAL BALL is LZO.

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Other records listing Kinamed, Inc. 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.

K122049NEUROPRO LOW PROFILE CRANIAL PLATING SYSTEMK072250SUPERCABLE GRIP AND PLATE SYSTEMK050897NAVIPRO SHOULDER SOFTWARE MODULEK033668NAVIPRO KNEE SOFTWARE MODULEK032950GEM INSET PATELLAR COMPONENTK030256ISO-ELASTIC CERCLAGE SYSTEM

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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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