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FDA PMA

Acid, hyaluronic, intraarticular

PMA Number: P180040 · 2024-06-28

ApplicantFidia Farmaceutici S.P.A.
Decision Date2024-06-28
PMA NumberP180040
Product CodeMOZ
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Acid, hyaluronic, intraarticular is the device name listed in this FDA 510(k) record. The listed applicant is Fidia Farmaceutici S.P.A.. It received FDA 510(k) clearance on 2024-06-28. The device is classified under product code MOZ. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Acid, hyaluronic, intraarticular?

Acid, hyaluronic, intraarticular is a medical device that received FDA 510(k) clearance on 2024-06-28. The listed applicant is Fidia Farmaceutici S.P.A..

When did Acid, hyaluronic, intraarticular receive FDA 510(k) clearance?

The clearance date for Acid, hyaluronic, intraarticular can be found in the official FDA records.

Who is the listed applicant for Acid, hyaluronic, intraarticular?

The FDA 510(k) record lists Fidia Farmaceutici S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Acid, hyaluronic, intraarticular?

The FDA product code for Acid, hyaluronic, intraarticular is MOZ.

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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