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).
| Device ID | K140142 |
| 510k Number | K140142 |
| Device Name: | CHOICE SPINE LUMBAR SPACER SYSTEM (SABRE, SHARK, HORNET, HARPOON) |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | CHOICE SPINE, LP 306 ERIN DRIVE Knoxville, TN 37919 -2141 |
| Contact | Kim Finch |
| Correspondent | Kim Finch CHOICE SPINE, LP 306 ERIN DRIVE Knoxville, TN 37919 -2141 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-01-22 |
| Decision Date | 2014-07-16 |
| Summary: | summary |