The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Choice Spine Lumbar Spacer System (sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Veo™ Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion System.
| Device ID | K153107 |
| 510k Number | K153107 |
| Device Name: | Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine VEO™ Lateral Access & Interbody Fusion System, Choice Spine Interbody Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | CHOICE SPINE, LP 400 Erin Drive Knoxville, TN 37919 |
| Contact | Kim Finch |
| Correspondent | Kim Finch CHOICE SPINE, LP 400 Erin Drive Knoxville, TN 37919 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-10-27 |
| Decision Date | 2016-05-19 |
| Summary: | summary |