Company ยท US
Innerspace, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2012. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 2, 2012 | K113088 | HUMMINGBIRD SUBDURAL H900DS (DRAINAGE AND ICP), HUMMINGBIRD SUBDURAL- H800S (ICP ONLY) Innerspace, Inc. | GWM |
| Sep 29, 2009 | K083378 | SYNERGY Innerspace, Inc. | GWM |
| Apr 29, 2008 | K072379 | MPS OXIPORT AND MPS OXIPORT PLUS Innerspace, Inc. | GWM |
| Mar 1, 2005 | K041838 | MPS (OR MPS-T) Innerspace, Inc. | GWM |
| Sep 9, 2002 | K013705 | ACT III VENTRICULAR CATHETER Innerspace, Inc. | GWM |
| Mar 8, 2002 | K013005 | ACT 11 MP VENTRICULAR CATHETER Innerspace, Inc. | HCA |
| Jun 28, 2001 | K010422 | ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER Innerspace, Inc. | GWM |
| Jun 15, 2001 | K003905 | ACTI-ICP MONITORING SYSTEM Innerspace, Inc. | GWM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||