NuVasive® Growth Rod Conversion Set
FDA 510(k) clearance K172979 · decided 2017-11-06
Clearance details
- K-number
- K172979
- Device name
- NuVasive® Growth Rod Conversion Set
- Applicant
- Nu Vasive, Incorporated
- Decision
- Substantially Equivalent
- Date received
- 2017-09-27
- Decision date
- 2017-11-06
- Days to decision
- 40 days
- Clearance type
- Traditional
- Product code
- PGM
- Device class
- 2
- Regulation number
- 888.3070
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- San Diego, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.