The following data is part of a premarket notification filed by Choice Spine, Lp. with the FDA for Tiger Shark™ System.
| Device ID | K172816 |
| 510k Number | K172816 |
| Device Name: | TiGer Shark™ 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 | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-18 |
| Decision Date | 2018-01-26 |
| Summary: | summary |