The following data is part of a premarket notification filed by Spinecraft, Inc. with the FDA for Apex Spine System 5.50 Mm Titanium Rod & Polyaxial Screw Washer.
| Device ID | K092825 |
| 510k Number | K092825 |
| Device Name: | APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | SPINECRAFT, INC. 2215 ENTREPRISE DR. Westchester, IL 60154 -5804 |
| Contact | Ami Akallal-asaad |
| Correspondent | Ami Akallal-asaad SPINECRAFT, INC. 2215 ENTREPRISE DR. Westchester, IL 60154 -5804 |
| Product Code | KWP |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-11 |
| Decision Date | 2010-03-16 |
| Summary: | summary |