FDA Device Intelligence
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Anchor, Suture, Bone Fixation, Metallic

FDA product code NOV · Class 2 · Orthopedic

8
Registered devices
30
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-06-17Integra LifeSciences Corp.Data from internal studies suggests there may be a potential that the secondary package seal integrity does not provide the level of sterility intended for Mini

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.