FDA 510(k) Applications Submitted by John Rossman
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161173 | 04/26/2016 | Avenue« T TLIF Cage | LDR SPINE USA, INC. |
| K163621 | 12/22/2016 | Vitoss Bioactive (BA) Injectable | Orthovita, Inc. |
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