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FDA 510(k)

MICRO-RING SYSTEM PRECISION ATTACH.

K-Number: K791788 · 1979-10-22

Decision Date1979-10-22
Product CodeEGG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICRO-RING SYSTEM PRECISION ATTACH. is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-10-22 under 510(k) number K791788. 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 SYSTEM PRECISION ATTACH.?

MICRO-RING SYSTEM PRECISION ATTACH. is a medical device that received FDA 510(k) clearance on 1979-10-22. The listed applicant is Howmedica Corp.. The 510(k) number is K791788.

When did MICRO-RING SYSTEM PRECISION ATTACH. receive FDA 510(k) clearance?

MICRO-RING SYSTEM PRECISION ATTACH. received FDA 510(k) clearance on 1979-10-22, under 510(k) number K791788.

Who is the listed applicant for MICRO-RING SYSTEM PRECISION ATTACH.?

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 SYSTEM PRECISION ATTACH.?

The FDA product code for MICRO-RING SYSTEM PRECISION ATTACH. is EGG.

Related Clinical Trials

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.

Other records listing Howmedica Corp. 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.

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Related Devices (Code: EGG)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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