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FDA 510(k)

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS

K-Number: K073067 · 2008-02-15

ApplicantDentsply International, Inc.
Decision Date2008-02-15
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS 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 2008-02-15 under 510(k) number K073067. 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 ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS?

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS is a medical device that received FDA 510(k) clearance on 2008-02-15. The listed applicant is Dentsply International, Inc.. The 510(k) number is K073067.

When did ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS receive FDA 510(k) clearance?

ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS received FDA 510(k) clearance on 2008-02-15, under 510(k) number K073067.

Who is the listed applicant for ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS?

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 DENTAL IMPLANT SYSTEM/CLAIMS?

The FDA product code for ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS is DZE.

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Related Devices (Code: DZE)

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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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