Siconus SI Joint Fixation System
FDA 510(k) clearance K162121 · decided 2017-01-18
Clearance details
- K-number
- K162121
- Device name
- Siconus SI Joint Fixation System
- Applicant
- Camber Spine Technologies
- Decision
- Substantially Equivalent
- Date received
- 2016-08-01
- Decision date
- 2017-01-18
- Days to decision
- 170 days
- Clearance type
- Traditional
- Product code
- OUR
- Device class
- 2
- Regulation number
- 888.3040
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Wayne, PA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.