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FDA 510(k)

IMPLANTIUM ABUTMENTS

K-Number: K052823 · 2006-02-21

ApplicantDentium, Inc.
Decision Date2006-02-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANTIUM ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dentium, Inc.. It received FDA 510(k) clearance on 2006-02-21 under 510(k) number K052823. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTIUM ABUTMENTS?

IMPLANTIUM ABUTMENTS is a medical device that received FDA 510(k) clearance on 2006-02-21. The listed applicant is Dentium, Inc.. The 510(k) number is K052823.

When did IMPLANTIUM ABUTMENTS receive FDA 510(k) clearance?

IMPLANTIUM ABUTMENTS received FDA 510(k) clearance on 2006-02-21, under 510(k) number K052823.

Who is the listed applicant for IMPLANTIUM ABUTMENTS?

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

What is the FDA product code for IMPLANTIUM ABUTMENTS?

The FDA product code for IMPLANTIUM ABUTMENTS is NHA.

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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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