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FDA 510(k)

FREEMAN ACETABULAR CUP

K-Number: K852699 · 1985-09-05

ApplicantAdvanced Biosearch Assn.
Decision Date1985-09-05
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FREEMAN ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biosearch Assn.. It received FDA 510(k) clearance on 1985-09-05 under 510(k) number K852699. 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 FREEMAN ACETABULAR CUP?

FREEMAN ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1985-09-05. The listed applicant is Advanced Biosearch Assn.. The 510(k) number is K852699.

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

FREEMAN ACETABULAR CUP received FDA 510(k) clearance on 1985-09-05, under 510(k) number K852699.

Who is the listed applicant for FREEMAN ACETABULAR CUP?

The FDA 510(k) record lists Advanced Biosearch Assn. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEMAN ACETABULAR CUP?

The FDA product code for FREEMAN ACETABULAR CUP is KWA.

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Other records listing Advanced Biosearch Assn. 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.

K905514AUTOGENESIS(TM) AUTOMATORK883888CATHSCANNER INTRAVASCULAR ULTRASONIC IMAGING SYST.K854770MARTIN LAMINAR OSTEOSYNTHESIS SYSTEMK855030CHAMPY BONE PLATES & BONE SCREWSK855031MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE PK853916P.M. HIP-FEMORAL PROSTHESIS

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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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