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FDA 510(k)

PRO-FEMUR R

K-Number: K003016 · 2000-12-13

ApplicantWrightmedicaltechnologyinc
Decision Date2000-12-13
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRO-FEMUR R is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2000-12-13 under 510(k) number K003016. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-FEMUR R?

PRO-FEMUR R is a medical device that received FDA 510(k) clearance on 2000-12-13. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K003016.

When did PRO-FEMUR R receive FDA 510(k) clearance?

PRO-FEMUR R received FDA 510(k) clearance on 2000-12-13, under 510(k) number K003016.

Who is the listed applicant for PRO-FEMUR R?

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

What is the FDA product code for PRO-FEMUR R?

The FDA product code for PRO-FEMUR R is LWJ.

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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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