NuVasive® Growth Rod Conversion Set— 510(k) K172979
Substantially EquivalentNu Vasive, Incorporated
FDA 510(k) clearance K172979 for NuVasive® Growth Rod Conversion Set, Substantially Equivalent on 2017-11-06. Applicant: Nu Vasive, Incorporated. Device class: 2.
Clearance details
- Applicant
- Nu Vasive, Incorporated
- Product code
- Code PGM
- Device class
- Class 2
- Regulation
- 21 CFR 888.3070
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
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More clearances from Nu Vasive, Incorporated
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