← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS III

NPT — Aortic Valve, Prosthesis, Percutaneously Delivered

To replace a patient's aortic heart valve. They are different from the classified device (heart valves) in that they are placed percutaneously and do not require open chest surgery or a cardiotomy for placement.

DEVICE CLASS
Class III
MEDICAL SPECIALTY
Unknown
REVIEW PANEL
CV
✓ Implant✓ Life-sustaining— GMP-exempt— Third-party review eligible
4
510(K)/PMA CLEARANCES
pma: 4
0
RECALL ENTRIES

Recent clearances

P140031Edwards Lifesciences, LLC · pma2026-07-17
P130021Medtronic, Inc. · pma2026-07-14
P190023ABBOTT MEDICAL · pma2026-07-09
P250024JenaValve Technology, Inc. · pma2026-07-09

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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