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FDA 510(k)

MODIFIED FREEMAN REVISION ACETABULAR CUP

K-Number: K902111 · 1990-08-22

ApplicantTurnkey Intergration USA, Inc.
Decision Date1990-08-22
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED FREEMAN REVISION ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1990-08-22 under 510(k) number K902111. 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 MODIFIED FREEMAN REVISION ACETABULAR CUP?

MODIFIED FREEMAN REVISION ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K902111.

When did MODIFIED FREEMAN REVISION ACETABULAR CUP receive FDA 510(k) clearance?

MODIFIED FREEMAN REVISION ACETABULAR CUP received FDA 510(k) clearance on 1990-08-22, under 510(k) number K902111.

Who is the listed applicant for MODIFIED FREEMAN REVISION ACETABULAR CUP?

The FDA 510(k) record lists Turnkey Intergration USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED FREEMAN REVISION ACETABULAR CUP?

The FDA product code for MODIFIED FREEMAN REVISION ACETABULAR CUP is KWA.

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Other records listing Turnkey Intergration USA, Inc. as applicant

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.

K991405OMNI-FIX, HUMERAL NAILK990523B2C, ESPACE REVISION CUP SYSTEMK990307OMNI-FIX, NAIL SYSTEMK972411LINK CEMENT PLUGK970284ARTOS, DIPLOS SYSTEMK970084LINK CERCLAGE WIRE SYSTEM

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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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