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FDA 510(k)

THE ORIGINAL LEINBACH PLATFORM TOTAL HIP

K-Number: K820755 · 1982-06-10

ApplicantAllo Pro Corp.
Decision Date1982-06-10
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE ORIGINAL LEINBACH PLATFORM TOTAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1982-06-10 under 510(k) number K820755. 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 THE ORIGINAL LEINBACH PLATFORM TOTAL HIP?

THE ORIGINAL LEINBACH PLATFORM TOTAL HIP is a medical device that received FDA 510(k) clearance on 1982-06-10. The listed applicant is Allo Pro Corp.. The 510(k) number is K820755.

When did THE ORIGINAL LEINBACH PLATFORM TOTAL HIP receive FDA 510(k) clearance?

THE ORIGINAL LEINBACH PLATFORM TOTAL HIP received FDA 510(k) clearance on 1982-06-10, under 510(k) number K820755.

Who is the listed applicant for THE ORIGINAL LEINBACH PLATFORM TOTAL HIP?

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

What is the FDA product code for THE ORIGINAL LEINBACH PLATFORM TOTAL HIP?

The FDA product code for THE ORIGINAL LEINBACH PLATFORM TOTAL HIP is KWL.

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Other records listing Allo Pro 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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