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FDA 510(k)

TROCHANTERIC NAIL

K-Number: K010780 · 2001-06-12

ApplicantDePuy Orthopaedics, Inc.
Decision Date2001-06-12
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TROCHANTERIC NAIL is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Orthopaedics, Inc.. It received FDA 510(k) clearance on 2001-06-12 under 510(k) number K010780. 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 TROCHANTERIC NAIL?

TROCHANTERIC NAIL is a medical device that received FDA 510(k) clearance on 2001-06-12. The listed applicant is DePuy Orthopaedics, Inc.. The 510(k) number is K010780.

When did TROCHANTERIC NAIL receive FDA 510(k) clearance?

TROCHANTERIC NAIL received FDA 510(k) clearance on 2001-06-12, under 510(k) number K010780.

Who is the listed applicant for TROCHANTERIC NAIL?

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

What is the FDA product code for TROCHANTERIC NAIL?

The FDA product code for TROCHANTERIC 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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