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 |