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FDA 510(k)

AUSTIN MOORE TYPE HIP PROSTHESIS

K-Number: K903241 · 1990-07-30

ApplicantOnyx Medical Corp.
Decision Date1990-07-30
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AUSTIN MOORE TYPE HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Onyx Medical Corp.. It received FDA 510(k) clearance on 1990-07-30 under 510(k) number K903241. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUSTIN MOORE TYPE HIP PROSTHESIS?

AUSTIN MOORE TYPE HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1990-07-30. The listed applicant is Onyx Medical Corp.. The 510(k) number is K903241.

When did AUSTIN MOORE TYPE HIP PROSTHESIS receive FDA 510(k) clearance?

AUSTIN MOORE TYPE HIP PROSTHESIS received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903241.

Who is the listed applicant for AUSTIN MOORE TYPE HIP PROSTHESIS?

The FDA 510(k) record lists Onyx Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUSTIN MOORE TYPE HIP PROSTHESIS?

The FDA product code for AUSTIN MOORE TYPE HIP PROSTHESIS is KWL.

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Other records listing Onyx Medical Corp. as applicant

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Related Devices (Code: KWL)

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.

K262290REMEDY POLY+PLUS SNAP FIT Acetabular CupOsteoremedies, LLCK260536Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone CementDepuy Ireland UCK253675OsteoRemedies Hip Spacer SystemOsteoremedies, LLCK252326InterSpace GV Hip SpacerTecres S.P.A.K242865Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder SpacerBiocomposites, Ltd.K234028COPAL® exchange G hip spacer; COPAL® G+VHeraeus Medical GmbH

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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