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Instrument, Surgical, Non-Powered

FDA product code HAO · Class 1 · Neurology

5,047
Registered devices
351
Adverse events
2
Recalls
34
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2011-04-04Zimmer Inc.A rounded or partially rounded tip on the screwdriver may not provide the required locking torque to lock the closure top to the polyaxial screw. When the hex t
2010-07-02Integra LifeSciences CorpCertain NeuroBalloon Catheters have the potential to improperly inflate or deflate under certain conditions.

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