Interventional Spine, Inc.
8 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Opticage(R) Expandable Interbody Fusion Device (K160464) | Interventional Spine, Inc. | 2016-04-04 |
| Opticage Expandable Interbody Fusion Device (K152156) | Interventional Spine, Inc. | 2015-10-19 |
| OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE (K140716) | Interventional Spine, Inc. | 2014-11-24 |
| OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070 (K133583) | Interventional Spine, Inc. | 2014-02-10 |
| OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00 (K132479) | Interventional Spine, Inc. | 2013-09-19 |
| OPTICAGE INTERBODY FUSION DEVICE (K113527) | Interventional Spine, Inc. | 2012-01-20 |
| PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER (K090767) | Interventional Spine, Inc. | 2009-06-11 |
| SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT (K082795) | Interventional Spine, Inc. | 2008-12-12 |
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Every clearance here is in the API, with alerts when new ones post.