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 |