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FDA 510(k)

CERTAIN PREVAIL DENTAL IMPLANT

K-Number: K061629 · 2007-02-23

Decision Date2007-02-23
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERTAIN PREVAIL DENTAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations, Inc.. It received FDA 510(k) clearance on 2007-02-23 under 510(k) number K061629. 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 CERTAIN PREVAIL DENTAL IMPLANT?

CERTAIN PREVAIL DENTAL IMPLANT is a medical device that received FDA 510(k) clearance on 2007-02-23. The listed applicant is Implant Innovations, Inc.. The 510(k) number is K061629.

When did CERTAIN PREVAIL DENTAL IMPLANT receive FDA 510(k) clearance?

CERTAIN PREVAIL DENTAL IMPLANT received FDA 510(k) clearance on 2007-02-23, under 510(k) number K061629.

Who is the listed applicant for CERTAIN PREVAIL DENTAL IMPLANT?

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

What is the FDA product code for CERTAIN PREVAIL DENTAL IMPLANT?

The FDA product code for CERTAIN PREVAIL 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 Implant Innovations, 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.

View all 51 devices →

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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