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FDA 510(k)

FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS

K-Number: K072730 · 2008-03-27

ApplicantDentsply Intl.
Decision Date2008-03-27
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 2008-03-27 under 510(k) number K072730. 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 FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS?

FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS is a medical device that received FDA 510(k) clearance on 2008-03-27. The listed applicant is Dentsply Intl.. The 510(k) number is K072730.

When did FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS receive FDA 510(k) clearance?

FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS received FDA 510(k) clearance on 2008-03-27, under 510(k) number K072730.

Who is the listed applicant for FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS?

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

What is the FDA product code for FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS?

The FDA product code for FRIADENT CERCON AND ANKYLOS CERCON BALANCE ABUTMENTS is NHA.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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