Innerspace, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113088 | HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY) | GWM | 2012-05-02 | View |
| 510(k) | K083378 | SYNERGY | GWM | 2009-09-29 | View |
| 510(k) | K072379 | MPS OXIPORT AND MPS OXIPORT PLUS | GWM | 2008-04-29 | View |
| 510(k) | K041838 | MPS (OR MPS-T) | GWM | 2005-03-01 | View |
| 510(k) | K013705 | ACT III VENTRICULAR CATHETER | GWM | 2002-09-09 | View |
| 510(k) | K013005 | ACT 11 MP VENTRICULAR CATHETER | HCA | 2002-03-08 | View |
| 510(k) | K010422 | ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER | GWM | 2001-06-28 | View |
| 510(k) | K003905 | ACTI-ICP MONITORING SYSTEM | GWM | 2001-06-15 | View |
No matching devices.
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