FDA 510(k) Applications Submitted by X-SPINE SYSTEMS, INC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K140079 |
01/13/2014 |
SILEX SACROILIAC JOINT FUSION SYSTEM |
X-SPINE SYSTEMS, INC |
K120832 |
03/19/2012 |
FORTEX PEDICLE SCREW SYSTEM |
X-SPINE SYSTEMS, INC |
K150834 |
03/30/2015 |
Atrax Anterior Cervical Plating System |
X-Spine Systems, Inc |
K131350 |
05/10/2013 |
CALIX LUMBAR SPINAL IMPLANT SYSTEM |
X-SPINE SYSTEMS, INC |
K112036 |
07/18/2011 |
CALIX PC SPINAL IMPLANT SYSTEM |
X-SPINE SYSTEMS, INC |
K122163 |
07/20/2012 |
CERTEX SPINAL IMPLANT SYSTEM |
X-SPINE SYSTEMS, INC |
K112592 |
09/07/2011 |
AXLE PEEK INTERSPINOUS FUSION SYSTEM |
X-SPINE SYSTEMS, INC |
K123932 |
12/20/2012 |
ZYGAFIX SPINAL FACET SCREW SYSTEM |
X-SPINE SYSTEMS, INC |
K133947 |
12/23/2013 |
IRIX-A LUMBAR INTEGRATED FUSION SYSTEM |
X-SPINE SYSTEMS, INC |
K133094 |
09/30/2013 |
CERTEX OCT SPINAL IMPLANT SYSTEM |
X-SPINE SYSTEMS, INC |
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