FDA 510(k) Applications Submitted by HAN FAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090176 |
01/23/2009 |
NUVASIVE ADJUSTABLE VERTEBRAL BODY REPLACEMENT SYSTEM |
NUVASIVE, INC. |
| K090298 |
02/06/2009 |
NUVASIVE NEURO VISION SYSTEM |
NUVASIVE, INC. |
| K090981 |
04/07/2009 |
MODIFICATION TO: NUVASIVE SPHERX SYSTEM |
NUVASIVE, INC. |
| K091071 |
04/14/2009 |
NUVASIVE LATERAL PLATE SYSTEM |
NUVASIVE, INC. |
| K091502 |
05/21/2009 |
NUVASIVE SPHERX II SYSTEM |
NUVASIVE, INC. |
| K091623 |
06/03/2009 |
LAMINOPLASTY FIXATION SYSTEM |
NUVASIVE, INC. |
| K083028 |
10/10/2008 |
MODIFICATION TO: NUVASIVE SPHERX II SYSTEM |
NUVASIVE, INC. |
| K083341 |
11/12/2008 |
NUVASIVE HELIX-T ACP SYSTEM |
NUVASIVE, INC. |
| K080568 |
02/29/2008 |
X-MESH EXPANDABLE CAGE SYSTEM |
DEPUY SPINE, INC. |
| K081432 |
05/21/2008 |
HEALOS II BONE GRAFT SUBSTITUTE |
DEPUY SPINE, INC. |
| K081758 |
06/20/2008 |
HEALOS FX INJECTABLE BONE GRAFT REPLACEMENT, MODELS 276175002, 276175005, 276175010, 276175015 |
DEPUY SPINE, INC. |
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