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FDA 510(k)

EXPAND. RETENTION ENDOSSEOUS IMPLANT

K-Number: K771858 · 1977-10-20

ApplicantA.L. Miller, Inc.
Decision Date1977-10-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EXPAND. RETENTION ENDOSSEOUS IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is A.L. Miller, Inc.. It received FDA 510(k) clearance on 1977-10-20 under 510(k) number K771858. 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 EXPAND. RETENTION ENDOSSEOUS IMPLANT?

EXPAND. RETENTION ENDOSSEOUS IMPLANT is a medical device that received FDA 510(k) clearance on 1977-10-20. The listed applicant is A.L. Miller, Inc.. The 510(k) number is K771858.

When did EXPAND. RETENTION ENDOSSEOUS IMPLANT receive FDA 510(k) clearance?

EXPAND. RETENTION ENDOSSEOUS IMPLANT received FDA 510(k) clearance on 1977-10-20, under 510(k) number K771858.

Who is the listed applicant for EXPAND. RETENTION ENDOSSEOUS IMPLANT?

The FDA 510(k) record lists A.L. Miller, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPAND. RETENTION ENDOSSEOUS IMPLANT?

The FDA product code for EXPAND. RETENTION ENDOSSEOUS IMPLANT is DZE.

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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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