The following data is part of a premarket notification filed by X-spine Systems, Inc. with the FDA for Xspan Laminoplasty Fixation System.
| Device ID | K160114 |
| 510k Number | K160114 |
| Device Name: | Xspan Laminoplasty Fixation System |
| Classification | Orthosis, Spine, Plate, Laminoplasty, Metal |
| Applicant | X-SPINE SYSTEMS, INC. 452 ALEXANDERSVILLE RD. Miamisburg, OH 45342 |
| Contact | Kriss Anderson |
| Correspondent | Kriss Anderson X-SPINE SYSTEMS, INC. 452 ALEXANDERSVILLE RD. Miamisburg, OH 45342 |
| Product Code | NQW |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-01-19 |
| Decision Date | 2016-03-15 |
| Summary: | summary |