FDA 510(k) Applications Submitted by INTEGRA LIFESCIENCES
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120600 | 02/28/2012 | DURAGEN SECURE DURAL REGNERATION MATRIX | INTEGRA LIFESCIENCES |
| K103742 | 12/23/2010 | ACCELL EVO3 (FORMERLY ACCELL A2I) | INTEGRA LIFESCIENCES |
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