FDA 510(k)

PERFECTA AND EXTEND

K-Number: K004032 · 2001-02-15

Decision Date2001-02-15

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

PERFECTA AND EXTEND is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2001-02-15 under 510(k) number K004032. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFECTA AND EXTEND?

PERFECTA AND EXTEND is a medical device that received FDA 510(k) clearance on 2001-02-15. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K004032.

When did PERFECTA AND EXTEND receive FDA 510(k) clearance?

PERFECTA AND EXTEND received FDA 510(k) clearance on 2001-02-15, under 510(k) number K004032.

Who is the listed applicant for PERFECTA AND EXTEND?

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 PERFECTA AND EXTEND?

The FDA product code for PERFECTA AND EXTEND is LPH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.