The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Spinefrontier A-cift Solofuse Cervical Intervertebral Fusion Device System.
| Device ID | K131880 |
| 510k Number | K131880 |
| Device Name: | SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Applicant | SPINEFRONTIER, INC. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
| Contact | Meredith May |
| Correspondent | Meredith May SPINEFRONTIER, INC. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
| Product Code | OVE |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-06-25 |
| Decision Date | 2014-01-03 |
| Summary: | summary |