FDA 510(k) Applications Submitted by INTERVENTIONAL SPINE, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090767 |
03/23/2009 |
PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER |
INTERVENTIONAL SPINE, INC. |
| K082795 |
09/23/2008 |
SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT |
INTERVENTIONAL SPINE, INC. |
| K160464 |
02/19/2016 |
Opticage(R) Expandable Interbody Fusion Device |
INTERVENTIONAL SPINE, INC. |
| K140716 |
03/21/2014 |
OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE |
INTERVENTIONAL SPINE, INC. |
| K152156 |
08/03/2015 |
Opticage Expandable Interbody Fusion Device |
INTERVENTIONAL SPINE, INC. |
| K132479 |
08/08/2013 |
OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00 |
INTERVENTIONAL SPINE, INC. |
| K133583 |
11/21/2013 |
OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070 |
INTERVENTIONAL SPINE, INC. |
| K113527 |
11/30/2011 |
OPTICAGE INTERBODY FUSION DEVICE |
INTERVENTIONAL SPINE, INC. |
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