The following data is part of a premarket notification filed by Captiva Spine, Inc. with the FDA for Tirbolox-c Cervical Ibfd.
| Device ID | K181229 |
| 510k Number | K181229 |
| Device Name: | TirboLOX-C Cervical IBFD |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | Captiva Spine, Inc. 967 N. Alternate A1A, Ste. 1 Jupiter, FL 33477 |
| Contact | Jackie Ferro |
| Correspondent | Jackie Ferro Captiva Spine, Inc. 967 N. Alternate A1A, Ste. 1 Jupiter, FL 33477 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-05-09 |
| Decision Date | 2018-09-19 |
| Summary: | summary |