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Novo Surgical Inc.

NOVO SURGICAL, INC. · Model UR6282-25 · UDI-DI 00842331137389

GCC Prescription
5
510(k) clearances
74
Adverse events (10 deaths)
5
Recalls
100
Facilities

Description

female catheter, 5 3/4" (14.6 cm), 14 fr.

Recalls

DateFirmReason
2013-07-31DePuy Spine, Inc.Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.
2013-07-31DePuy Spine, Inc.Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.
2013-07-31DePuy Spine, Inc.Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.
2013-07-31DePuy Spine, Inc.Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.
2013-07-31DePuy Spine, Inc.Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.