NuVasive Modulus ALIF System
FDA 510(k) clearance K210271 · decided 2021-03-01
Clearance details
- K-number
- K210271
- Device name
- NuVasive Modulus ALIF System
- Applicant
- Nu Vasive, Incorporated
- Decision
- Substantially Equivalent
- Date received
- 2021-02-01
- Decision date
- 2021-03-01
- Days to decision
- 28 days
- Clearance type
- Special
- Product code
- OVD
- Device class
- 2
- Regulation number
- 888.3080
- 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.