NuVasiveNVM5 System— 510(k) K152942
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K152942 for NuVasiveNVM5 System, Substantially Equivalent on 2016-01-13. Applicant: Nu Vasive, Incorporated. Device class: 2.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code PDQ
view all- K260992 — iD3 Nav Decompression Probe (NTX-9005); iD3 Ball Tip Stim Probe (NTX-9006); iD3 Nav Ball Tip Probe (NTX-9007)
- K253580 — Sterile Insulated Dilators, 5, 10, 16mm (MDT-0442S); Sterile, Insulated Dilator, 20mm (MDT-0469S)
- K243636 — Neuralytix iD3 System (NTX-9001)
- K223438 — TELIGEN System Peripheral Motor Nerve Stimulation Indications
- K221821 — ATEC IOM Accessory Instruments
More clearances from Nu Vasive, Incorporated
view allData sourced from openFDA. This site is unofficial and independent of the FDA.