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FDA 510(k)

EXETER BONE LAUAGE SYSTEM

K-Number: K790811 · 1979-07-30

ApplicantHowmedica Corp.
Decision Date1979-07-30
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EXETER BONE LAUAGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-07-30 under 510(k) number K790811. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXETER BONE LAUAGE SYSTEM?

EXETER BONE LAUAGE SYSTEM is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Howmedica Corp.. The 510(k) number is K790811.

When did EXETER BONE LAUAGE SYSTEM receive FDA 510(k) clearance?

EXETER BONE LAUAGE SYSTEM received FDA 510(k) clearance on 1979-07-30, under 510(k) number K790811.

Who is the listed applicant for EXETER BONE LAUAGE SYSTEM?

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 EXETER BONE LAUAGE SYSTEM?

The FDA product code for EXETER BONE LAUAGE SYSTEM is FQH.

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Other records listing Howmedica Corp. as applicant

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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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