FDA PMA

STENT, CORONARY

PMA Number: P020047 · 2023-06-14

ApplicantAbbott Vascular

Decision Date2023-06-14

PMA NumberP020047

Product CodeMAF

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

STENT, CORONARY is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Vascular. It received FDA 510(k) clearance on 2023-06-14. The device is classified under product code MAF. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the STENT, CORONARY?

STENT, CORONARY is a medical device that received FDA 510(k) clearance on 2023-06-14. The listed applicant is Abbott Vascular.

When did STENT, CORONARY receive FDA 510(k) clearance?

The clearance date for STENT, CORONARY can be found in the official FDA records.

Who is the listed applicant for STENT, CORONARY?

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

What is the FDA product code for STENT, CORONARY?

The FDA product code for STENT, CORONARY is MAF.

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.