LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM
FDA 510(k) clearance K051275 · decided 2005-12-09
Clearance details
- K-number
- K051275
- Device name
- LAGUNA MONOAXIAL PEDICLE SCREW SYSTEM
- Applicant
- Allez Spine, LLC
- Decision
- Substantially Equivalent
- Date received
- 2005-05-17
- Decision date
- 2005-12-09
- Days to decision
- 206 days
- Clearance type
- Special
- Product code
- NKB
- Device class
- 2
- Regulation number
- 888.3070
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Cardiff, CA, US
- Third-party review
- No
- Expedited review
- No
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