The following data is part of a premarket notification filed by Spinecraft, Inc. with the FDA for Apex Spine System.
| Device ID | K062513 |
| 510k Number | K062513 |
| Device Name: | APEX SPINE SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | SPINECRAFT, INC. 2215 ENTERPRISE DRIVE SUITE 1504 Westchester, IL 60154 |
| Contact | Ami Akallal-asaad |
| Correspondent | Ami Akallal-asaad SPINECRAFT, INC. 2215 ENTERPRISE DRIVE SUITE 1504 Westchester, IL 60154 |
| Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-28 |
| Decision Date | 2006-12-22 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() APEX SPINE SYSTEM 85820194 not registered Dead/Abandoned |
SpineCraft, LLC 2013-01-10 |