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FDA 510(k)

PROFEMUR TL CLASSIC HIP STEM

K-Number: K123688 · 2013-02-08

ApplicantWrightmedicaltechnologyinc
Decision Date2013-02-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROFEMUR TL CLASSIC HIP STEM is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2013-02-08 under 510(k) number K123688. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROFEMUR TL CLASSIC HIP STEM?

PROFEMUR TL CLASSIC HIP STEM is a medical device that received FDA 510(k) clearance on 2013-02-08. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K123688.

When did PROFEMUR TL CLASSIC HIP STEM receive FDA 510(k) clearance?

PROFEMUR TL CLASSIC HIP STEM received FDA 510(k) clearance on 2013-02-08, under 510(k) number K123688.

Who is the listed applicant for PROFEMUR TL CLASSIC HIP STEM?

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 PROFEMUR TL CLASSIC HIP STEM?

The FDA product code for PROFEMUR TL CLASSIC HIP STEM is LZO.

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Related Devices (Code: LZO)

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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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