The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Fixation System.
| Device ID | K121850 |
| 510k Number | K121850 |
| Device Name: | CHOICE SPINE FIXATION SYSTEM |
| Classification | System, Facet Screw Spinal Device |
| Applicant | CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
| Contact | Kim Finch |
| Correspondent | Kim Finch CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
| Product Code | MRW |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-25 |
| Decision Date | 2012-09-20 |
| Summary: | summary |