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FDA 510(k)

MICRO-RING

K-Number: K780711 · 1978-05-26

ApplicantHowmedica Corp.
Decision Date1978-05-26
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO-RING is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780711. The device is classified under product code EGG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-RING?

MICRO-RING is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Howmedica Corp.. The 510(k) number is K780711.

When did MICRO-RING receive FDA 510(k) clearance?

MICRO-RING received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780711.

Who is the listed applicant for MICRO-RING?

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 MICRO-RING?

The FDA product code for MICRO-RING is EGG.

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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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