The following data is part of a premarket notification filed by Spine Wave, Inc. with the FDA for Sniper (r) Spine System.
| Device ID | K160003 |
| 510k Number | K160003 |
| Device Name: | Sniper (R) Spine System |
| Classification | Orthosis, Spinal Pedicle Fixation |
| Applicant | SPINE WAVE, INC. 3 ENTERPRISE DRIVE SUITE 210 Shelton, CT 06484 |
| Contact | Kelly Barbieri |
| Correspondent | Kelly Barbieri SPINE WAVE, INC. 3 ENTERPRISE DRIVE SUITE 210 Shelton, CT 06484 |
| Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-01-04 |
| Decision Date | 2016-02-26 |
| Summary: | summary |