FDA Product Code
FDA Product Code OQB — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Orthopedic
- 21 CFR Citation
- 888.3085
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K251302 | OptiMesh Multiplanar Expandable Interbody Fusion System | Spineology, Inc. | 2025-12-15 | Traditional | PDF ↗ |
| K230927 | OptiMesh Multiplanar Expandable Interbody Fusion System | Spineology, Inc. | 2023-11-01 | Traditional | PDF ↗ |
| K231781 | OptiMesh Multiplanar Expandable Interbody Fusion System | Spineology, Inc. | 2023-10-18 | Special | PDF ↗ |
| DEN200010 | Spineology Interbody Fusion System | Spineology, Inc. | 2020-09-18 | Direct | — |
Product code OQB · Class II · Orthopedic. Data: openFDA.