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FDA 510(k)

PROFEMUR HIP SYSTEM MODULAR NECKS

K-Number: K100866 · 2010-04-28

ApplicantWrightmedicaltechnologyinc
Decision Date2010-04-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROFEMUR HIP SYSTEM MODULAR NECKS is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2010-04-28 under 510(k) number K100866. 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 HIP SYSTEM MODULAR NECKS?

PROFEMUR HIP SYSTEM MODULAR NECKS is a medical device that received FDA 510(k) clearance on 2010-04-28. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K100866.

When did PROFEMUR HIP SYSTEM MODULAR NECKS receive FDA 510(k) clearance?

PROFEMUR HIP SYSTEM MODULAR NECKS received FDA 510(k) clearance on 2010-04-28, under 510(k) number K100866.

Who is the listed applicant for PROFEMUR HIP SYSTEM MODULAR NECKS?

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 HIP SYSTEM MODULAR NECKS?

The FDA product code for PROFEMUR HIP SYSTEM MODULAR NECKS is 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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