FDA 510(k) Applications Submitted by SPINE VIEW, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K120680 |
03/06/2012 |
ENSPIRE DISCECTOMY SYSTEM |
SPINE VIEW, INC. |
K121548 |
05/25/2012 |
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS) |
SPINE VIEW, INC. |
K160856 |
03/28/2016 |
SpineView X-Pac Expandable Lumbar Cage System |
Spine View, Inc. |
K110992 |
04/08/2011 |
ENSPIRE DEBRIDER SYSTEM |
SPINE VIEW, INC. |
K122134 |
07/18/2012 |
FLEXLITE CAMERA |
SPINE VIEW, INC. |
K152539 |
09/04/2015 |
SpineView X-Pac Expandable Lumbar Cage System |
SPINE VIEW, INC. |
K081051 |
04/14/2008 |
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS), SPINEVU MINISCOPE |
SPINE VIEW, INC. |
K090278 |
02/04/2009 |
ENSPIRE DEBRIDER SYSTEM |
SPINE VIEW, INC. |
K113362 |
11/15/2011 |
SPINEVU ENDOSCOPIC SPINE SYSTEM (SESS) |
SPINE VIEW, INC. |
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