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FDA 510(k)

KINAMED CEMENTED CTH STEM

K-Number: K902074 · 1990-06-08

ApplicantKinamed, Inc.
Decision Date1990-06-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

KINAMED CEMENTED CTH STEM is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 1990-06-08 under 510(k) number K902074. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the KINAMED CEMENTED CTH STEM?

KINAMED CEMENTED CTH STEM is a medical device that received FDA 510(k) clearance on 1990-06-08. The listed applicant is Kinamed, Inc.. The 510(k) number is K902074.

When did KINAMED CEMENTED CTH STEM receive FDA 510(k) clearance?

KINAMED CEMENTED CTH STEM received FDA 510(k) clearance on 1990-06-08, under 510(k) number K902074.

Who is the listed applicant for KINAMED CEMENTED CTH STEM?

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 CEMENTED CTH STEM?

The FDA product code for KINAMED CEMENTED CTH STEM 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.

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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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