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FDA 510(k)

INTERPLANTS

K-Number: K771366 · 1977-08-03

ApplicantMaurices J. Fagan, Jr. B.S., D.D.S.
Decision Date1977-08-03
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Maurices J. Fagan, Jr. B.S., D.D.S.. It received FDA 510(k) clearance on 1977-08-03 under 510(k) number K771366. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERPLANTS?

INTERPLANTS is a medical device that received FDA 510(k) clearance on 1977-08-03. The listed applicant is Maurices J. Fagan, Jr. B.S., D.D.S.. The 510(k) number is K771366.

When did INTERPLANTS receive FDA 510(k) clearance?

INTERPLANTS received FDA 510(k) clearance on 1977-08-03, under 510(k) number K771366.

Who is the listed applicant for INTERPLANTS?

The FDA 510(k) record lists Maurices J. Fagan, Jr. B.S., D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTERPLANTS?

The FDA product code for INTERPLANTS is DZE.

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Related Devices (Code: DZE)

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

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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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