FDA 510(k) Applications Submitted by JANET M WEBB
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131061 | 04/16/2013 | RESTORE BUNION CORRECTION SYSTEM | NEXTREMITY SOLUTIONS |
| K090707 | 03/17/2009 | TALOS INTERVERTEBRAL BODY FUSION DEVICE | MEDITECH ADVISORS, LLC |
| K051027 | 04/22/2005 | STALIF TT | SURGICRAFT LTD. |
| K041469 | 06/02/2004 | ANTERIOR COMPACT SYSTEM | X-SPINE SYSTEMS |
| K041617 | 06/15/2004 | STALIF TT | SURGICRAFT LTD. |
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