The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Blackbird Spinal System.
| Device ID | K133214 |
| 510k Number | K133214 |
| Device Name: | BLACKBIRD SPINAL SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| 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 | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-10-18 |
| Decision Date | 2014-03-07 |
| Summary: | summary |