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FDA 510(k)

CORIN THOMPSON PROSTHESIS, MODIFICATION

K-Number: K931753 · 1994-10-07

ApplicantCorin Orthopedic Products
Decision Date1994-10-07
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

CORIN THOMPSON PROSTHESIS, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Corin Orthopedic Products. It received FDA 510(k) clearance on 1994-10-07 under 510(k) number K931753. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CORIN THOMPSON PROSTHESIS, MODIFICATION?

CORIN THOMPSON PROSTHESIS, MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-10-07. The listed applicant is Corin Orthopedic Products. The 510(k) number is K931753.

When did CORIN THOMPSON PROSTHESIS, MODIFICATION receive FDA 510(k) clearance?

CORIN THOMPSON PROSTHESIS, MODIFICATION received FDA 510(k) clearance on 1994-10-07, under 510(k) number K931753.

Who is the listed applicant for CORIN THOMPSON PROSTHESIS, MODIFICATION?

The FDA 510(k) record lists Corin Orthopedic Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORIN THOMPSON PROSTHESIS, MODIFICATION?

The FDA product code for CORIN THOMPSON PROSTHESIS, MODIFICATION is KWL.

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Other records listing Corin Orthopedic Products 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.

K931752CORIN AUSTIN-MOORE PROSTHESIS, MODIFICATIONK934166NUFFIELD TOTAL KNEE UHMWPE TIBIA (ONE PIECE) MODIFICATIONK925866CENATOR TOTAL HIP SYSTEMK925897CORIN BIPOLAR PROSTHESIS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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