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FDA 510(k)

CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL

K-Number: K041425 · 2004-06-25

ApplicantWrightmedicaltechnologyinc
Decision Date2004-06-25
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Wrightmedicaltechnologyinc. It received FDA 510(k) clearance on 2004-06-25 under 510(k) number K041425. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL?

CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL is a medical device that received FDA 510(k) clearance on 2004-06-25. The listed applicant is Wrightmedicaltechnologyinc. The 510(k) number is K041425.

When did CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL receive FDA 510(k) clearance?

CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL received FDA 510(k) clearance on 2004-06-25, under 510(k) number K041425.

Who is the listed applicant for CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL?

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 CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL?

The FDA product code for CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL is KWA.

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Related Devices (Code: KWA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K122778PROFEMUR Z REVISION HIP STEMWrightmedicaltechnologyincK121544DYNASTY BIOFOAM SHELLWrightmedicaltechnologyincK113271METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONSBiomet Manufacturing, Inc.K113322CONSERVE THIN SHELLWrightmedicaltechnologyincK112080PRESERVE HIP STEMWrightmedicaltechnologyincK112150PROFEMUR GLADIATOR HA HIP STEMWrightmedicaltechnologyinc

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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