The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Vertebral Body Replacement (vbr) Device System.
| Device ID | K120570 |
| 510k Number | K120570 |
| Device Name: | CHOICE SPINE VERTEBRAL BODY REPLACEMENT (VBR) DEVICE SYSTEM |
| Classification | Spinal Vertebral Body Replacement Device |
| Applicant | CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
| Contact | Mark Bekkala |
| Correspondent | Mark Bekkala CHOICE SPINE, LP 400 Erin Dr Knoxville, TN 37919 |
| Product Code | MQP |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-02-27 |
| Decision Date | 2012-04-05 |
| Summary: | summary |