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FDA PMA

Prosthesis, metatarsophalangeal joint cartilage replacement implant

PMA Number: P150017 · 2021-12-10

ApplicantCartiva, Inc.
Decision Date2021-12-10
PMA NumberP150017
Product CodePNW
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Prosthesis, metatarsophalangeal joint cartilage replacement implant is the device name listed in this FDA 510(k) record. The listed applicant is Cartiva, Inc.. It received FDA 510(k) clearance on 2021-12-10. The device is classified under product code PNW. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Prosthesis, metatarsophalangeal joint cartilage replacement implant?

Prosthesis, metatarsophalangeal joint cartilage replacement implant is a medical device that received FDA 510(k) clearance on 2021-12-10. The listed applicant is Cartiva, Inc..

When did Prosthesis, metatarsophalangeal joint cartilage replacement implant receive FDA 510(k) clearance?

The clearance date for Prosthesis, metatarsophalangeal joint cartilage replacement implant can be found in the official FDA records.

Who is the listed applicant for Prosthesis, metatarsophalangeal joint cartilage replacement implant?

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

What is the FDA product code for Prosthesis, metatarsophalangeal joint cartilage replacement implant?

The FDA product code for Prosthesis, metatarsophalangeal joint cartilage replacement implant is PNW.

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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