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FDA 510(k)

ANKYLOS TEMPORARY ABUTMENT BALANCE

K-Number: K073073 · 2008-02-12

ApplicantDentsply International, Inc.
Decision Date2008-02-12
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANKYLOS TEMPORARY ABUTMENT BALANCE is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply International, Inc.. It received FDA 510(k) clearance on 2008-02-12 under 510(k) number K073073. 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 ANKYLOS TEMPORARY ABUTMENT BALANCE?

ANKYLOS TEMPORARY ABUTMENT BALANCE is a medical device that received FDA 510(k) clearance on 2008-02-12. The listed applicant is Dentsply International, Inc.. The 510(k) number is K073073.

When did ANKYLOS TEMPORARY ABUTMENT BALANCE receive FDA 510(k) clearance?

ANKYLOS TEMPORARY ABUTMENT BALANCE received FDA 510(k) clearance on 2008-02-12, under 510(k) number K073073.

Who is the listed applicant for ANKYLOS TEMPORARY ABUTMENT BALANCE?

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

What is the FDA product code for ANKYLOS TEMPORARY ABUTMENT BALANCE?

The FDA product code for ANKYLOS TEMPORARY ABUTMENT BALANCE 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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