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FDA 510(k)

KINAMED CEMENTED ATH-LONG STEM

K-Number: K902073 · 1990-06-08

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

Device Summary

KINAMED CEMENTED ATH-LONG 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 K902073. 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 CEMENTED ATH-LONG STEM?

KINAMED CEMENTED ATH-LONG 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 K902073.

When did KINAMED CEMENTED ATH-LONG STEM receive FDA 510(k) clearance?

KINAMED CEMENTED ATH-LONG STEM received FDA 510(k) clearance on 1990-06-08, under 510(k) number K902073.

Who is the listed applicant for KINAMED CEMENTED ATH-LONG 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 ATH-LONG STEM?

The FDA product code for KINAMED CEMENTED ATH-LONG STEM is LZO.

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Other records listing Kinamed, Inc. as applicant

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Related Devices (Code: LZO)

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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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