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FDA 510(k)

ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL

K-Number: K082770 · 2008-12-11

ApplicantZimmer, Inc.
Decision Date2008-12-11
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2008-12-11 under 510(k) number K082770. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL?

ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL is a medical device that received FDA 510(k) clearance on 2008-12-11. The listed applicant is Zimmer, Inc.. The 510(k) number is K082770.

When did ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL receive FDA 510(k) clearance?

ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL received FDA 510(k) clearance on 2008-12-11, under 510(k) number K082770.

Who is the listed applicant for ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL?

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

What is the FDA product code for ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL?

The FDA product code for ZIMMER NATURAL NAIL SYSTEM TIBIAL NAIL is HSB.

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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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