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FDA 510(k)

2MM PEDIATRIC FLEX NAIL

K-Number: K022531 · 2002-08-26

ApplicantBiomet, Inc.
Decision Date2002-08-26
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

2MM PEDIATRIC FLEX NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2002-08-26 under 510(k) number K022531. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2MM PEDIATRIC FLEX NAIL?

2MM PEDIATRIC FLEX NAIL is a medical device that received FDA 510(k) clearance on 2002-08-26. The listed applicant is Biomet, Inc.. The 510(k) number is K022531.

When did 2MM PEDIATRIC FLEX NAIL receive FDA 510(k) clearance?

2MM PEDIATRIC FLEX NAIL received FDA 510(k) clearance on 2002-08-26, under 510(k) number K022531.

Who is the listed applicant for 2MM PEDIATRIC FLEX NAIL?

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

What is the FDA product code for 2MM PEDIATRIC FLEX NAIL?

The FDA product code for 2MM PEDIATRIC FLEX NAIL is HTY.

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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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