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FDA PMA

Implant, resorbable, for articular osteochondral repair

PMA Number: P210034 · 2026-06-04

ApplicantSmith and Nephew, Inc.
Decision Date2026-06-04
PMA NumberP210034
Product CodeQRU
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Implant, resorbable, for articular osteochondral repair is the device name listed in this FDA 510(k) record. The listed applicant is Smith and Nephew, Inc.. It received FDA 510(k) clearance on 2026-06-04. The device is classified under product code QRU. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Implant, resorbable, for articular osteochondral repair?

Implant, resorbable, for articular osteochondral repair is a medical device that received FDA 510(k) clearance on 2026-06-04. The listed applicant is Smith and Nephew, Inc..

When did Implant, resorbable, for articular osteochondral repair receive FDA 510(k) clearance?

The clearance date for Implant, resorbable, for articular osteochondral repair can be found in the official FDA records.

Who is the listed applicant for Implant, resorbable, for articular osteochondral repair?

The FDA 510(k) record lists Smith and Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Implant, resorbable, for articular osteochondral repair?

The FDA product code for Implant, resorbable, for articular osteochondral repair is QRU.

Related Clinical Trials

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.

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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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