FDA 510(k) Applications Submitted by DAVID J MCILHENNY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K081439 | 05/22/2008 | VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE | ORTHOVITA, INC. |
| K032812 | 09/09/2003 | ENDOSKELETON TA VERTEBRAL BODY REPLACEMENT | ORTHOVITA, INC. |
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