SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE
FDA 510(k) clearance K110933 · decided 2011-06-13
Clearance details
- K-number
- K110933
- Device name
- SPINEOLOGY PEEK LUMBAR INTERBODY FUSION DEVICE
- Applicant
- Spineology, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2011-04-04
- Decision date
- 2011-06-13
- Days to decision
- 70 days
- Clearance type
- Traditional
- Product code
- MAX
- Device class
- 2
- Regulation number
- 888.3080
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Saint Paul, MN, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.