NuVasive Next Generation NVM5 System— 510(k) K162313
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K162313 for NuVasive Next Generation NVM5 System, Substantially Equivalent on 2017-03-16. Applicant: Nu Vasive, Incorporated.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code PDQ
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.