NuVasive® VersaTie System— 510(k) K161265
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K161265 for NuVasive® VersaTie System, Substantially Equivalent on 2016-07-15. Applicant: Nu Vasive, Incorporated.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code OWI
- Advisory panel
- Orthopedic
- 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.