The following data is part of a premarket notification filed by Choice Spine, Lp with the FDA for Harrier-sa™ Lumbar Interbody System.
| Device ID | K180519 |
| 510k Number | K180519 |
| Device Name: | HARRIER-SA™ Lumbar Interbody System |
| Classification | Intervertebral Fusion Device With Integrated Fixation, 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 | OVD |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-02-27 |
| Decision Date | 2018-05-16 |
| Summary: | summary |