FDA 510(k) Applications Submitted by TRAVIS AROLA
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K080418 |
02/15/2008 |
REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST |
REGENERATION TECHNOLOGIES, INC. |
K091142 |
04/20/2009 |
TUTOPATCH, TUTOMESH, MODELS 68350, 68351, 68352, 68353, 68354, 68355, 68356, 68357, 68358 |
RTI BIOLOGICS, INC. |
K081538 |
06/02/2008 |
TUTOPATCH, TUTOMESH |
RTI BIOLOGICS, INC. |
K072238 |
08/13/2007 |
BIOSET XCH |
REGENERATION TECHNOLOGIES, INC. |
K073097 |
11/01/2007 |
TUTODENT DENTAL MEMBRANE |
TUTOGEN MEDICAL U.S., INC. |
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