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FDA 510(k)

TITANIUM PEDIATRIC FEMORAL NAIL

K-Number: K993956 · 1999-12-20

ApplicantBiomet, Inc.
Decision Date1999-12-20
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM PEDIATRIC FEMORAL 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 1999-12-20 under 510(k) number K993956. 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 TITANIUM PEDIATRIC FEMORAL NAIL?

TITANIUM PEDIATRIC FEMORAL NAIL is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Biomet, Inc.. The 510(k) number is K993956.

When did TITANIUM PEDIATRIC FEMORAL NAIL receive FDA 510(k) clearance?

TITANIUM PEDIATRIC FEMORAL NAIL received FDA 510(k) clearance on 1999-12-20, under 510(k) number K993956.

Who is the listed applicant for TITANIUM PEDIATRIC FEMORAL 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 TITANIUM PEDIATRIC FEMORAL NAIL?

The FDA product code for TITANIUM PEDIATRIC FEMORAL NAIL is HSB.

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Related Devices (Code: 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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