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Neurosurgical Nerve Locator
FDA product code PDQ · Class 2 · Ear, Nose, Throat
491
Registered devices
77
Adverse events
2
Recalls
36
510(k) clearances
Devices with this code
Guidance — Nuvasive, Inc.NVJJB — Nuvasive, Inc.PULSE — Nuvasive, Inc.Boston Endo Surgical Technologies LLC — Lacey Manufacturing Company, LLCFresh Whole Blood Donor Transfusion Set — Safeguard US Operating, LLCNVM5 — Nuvasive, Inc.NVM5 — Nuvasive, Inc.SafeOp — ALPHATEC SPINE, INC.ALARA Neuro Access Needle Kit — SURGENTEC, LLCPULSE — Nuvasive, Inc.SeaSpine — TEDAN SURGICAL INNOVATIONS, L.L.C.Remote Monitoring — Nuvasive, Inc.Site Prep Locator - Row Series — SURGENTEC, LLCPULSE — Nuvasive, Inc.Boston Endo Surgical Technologies LLC — Lacey Manufacturing Company, LLCPULSE — Nuvasive, Inc.SafeOp 3 — ALPHATEC SPINE, INC.NVM5 — Nuvasive, Inc.PULSE — Nuvasive, Inc.Bendini — Nuvasive, Inc.PULSE — Nuvasive, Inc.NVM5 — Nuvasive, Inc.NVM5 — Nuvasive, Inc.TELIGEN — Medos International Sàrl
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-06-23 | The Magstim Company Limited | Reports that manipulation of the cable which connects the pre-amplifier to the nerve monitor, and the cable which connects the pre-amplifier to the stimulator p |
| 2020-06-10 | NuVasive Inc | The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP ha |
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