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FDA 510(k)

G4 SLEEVED NAIL

K-Number: K020962 · 2002-05-24

ApplicantBiomet Manufacturing, Inc.
Decision Date2002-05-24
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

G4 SLEEVED NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing, Inc.. It received FDA 510(k) clearance on 2002-05-24 under 510(k) number K020962. 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 G4 SLEEVED NAIL?

G4 SLEEVED NAIL is a medical device that received FDA 510(k) clearance on 2002-05-24. The listed applicant is Biomet Manufacturing, Inc.. The 510(k) number is K020962.

When did G4 SLEEVED NAIL receive FDA 510(k) clearance?

G4 SLEEVED NAIL received FDA 510(k) clearance on 2002-05-24, under 510(k) number K020962.

Who is the listed applicant for G4 SLEEVED NAIL?

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

What is the FDA product code for G4 SLEEVED NAIL?

The FDA product code for G4 SLEEVED 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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