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FDA 510(k)

BROOKER FEMORAL NAILS

K-Number: K002278 · 2000-10-23

ApplicantBiomet Orthopedics, Inc.
Decision Date2000-10-23
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BROOKER FEMORAL NAILS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2000-10-23 under 510(k) number K002278. 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 BROOKER FEMORAL NAILS?

BROOKER FEMORAL NAILS is a medical device that received FDA 510(k) clearance on 2000-10-23. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K002278.

When did BROOKER FEMORAL NAILS receive FDA 510(k) clearance?

BROOKER FEMORAL NAILS received FDA 510(k) clearance on 2000-10-23, under 510(k) number K002278.

Who is the listed applicant for BROOKER FEMORAL NAILS?

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

What is the FDA product code for BROOKER FEMORAL NAILS?

The FDA product code for BROOKER FEMORAL NAILS 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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