FDA Device Intelligence
HomeDevice types › NDE

Rod, Fixation, Intramedullary And Accessories, Metallic And Non-Collapsible

FDA product code NDE · Class 2 · Orthopedic

7
Registered devices
4
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-11-09Stryker Howmedica Osteonics Corp.A review of packaging revealed the seal integrity of the pouch may be compromised. More specifically, there is a potential that the sterile pouch is not sealed

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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.