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FDA PMA

Prosthesis, finger, semi-constrained, metal/polymer

PMA Number: P240020 · 2026-06-24

ApplicantKeri Medical SA
Decision Date2026-06-24
PMA NumberP240020
Product CodeSFA
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Prosthesis, finger, semi-constrained, metal/polymer is the device name listed in this FDA 510(k) record. The listed applicant is Keri Medical SA. It received FDA 510(k) clearance on 2026-06-24. The device is classified under product code SFA. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Prosthesis, finger, semi-constrained, metal/polymer?

Prosthesis, finger, semi-constrained, metal/polymer is a medical device that received FDA 510(k) clearance on 2026-06-24. The listed applicant is Keri Medical SA.

When did Prosthesis, finger, semi-constrained, metal/polymer receive FDA 510(k) clearance?

The clearance date for Prosthesis, finger, semi-constrained, metal/polymer can be found in the official FDA records.

Who is the listed applicant for Prosthesis, finger, semi-constrained, metal/polymer?

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

What is the FDA product code for Prosthesis, finger, semi-constrained, metal/polymer?

The FDA product code for Prosthesis, finger, semi-constrained, metal/polymer is SFA.

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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