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FDA 510(k)

EVOLVE MODULAR RADIAL HEAD

K-Number: K060731 · 2006-04-19

ApplicantWrightmedicaltechnologyinc
Decision Date2006-04-19
Product CodeKWI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EVOLVE MODULAR RADIAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2006-04-19 under 510(k) number K060731. The device is classified under product code KWI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVOLVE MODULAR RADIAL HEAD?

EVOLVE MODULAR RADIAL HEAD is a medical device that received FDA 510(k) clearance on 2006-04-19. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K060731.

When did EVOLVE MODULAR RADIAL HEAD receive FDA 510(k) clearance?

EVOLVE MODULAR RADIAL HEAD received FDA 510(k) clearance on 2006-04-19, under 510(k) number K060731.

Who is the listed applicant for EVOLVE MODULAR RADIAL HEAD?

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 EVOLVE MODULAR RADIAL HEAD?

The FDA product code for EVOLVE MODULAR RADIAL HEAD is KWI.

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Related Devices (Code: KWI)

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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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