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FDA 510(k)

OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT

K-Number: K864995 · 1987-02-25

Decision Date1987-02-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Vent-Plant Corporation, Inc.. It received FDA 510(k) clearance on 1987-02-25 under 510(k) number K864995. 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 OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT?

OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 1987-02-25. The listed applicant is Vent-Plant Corporation, Inc.. The 510(k) number is K864995.

When did OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT receive FDA 510(k) clearance?

OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT received FDA 510(k) clearance on 1987-02-25, under 510(k) number K864995.

Who is the listed applicant for OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT?

The FDA 510(k) record lists Vent-Plant Corporation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT?

The FDA product code for OSSEOINTEGRATED FIXTURES FOR USE IN DENTAL IMPLANT is DZE.

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 Vent-Plant Corporation, Inc. 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.

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.

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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