FDA 510(k) Applications Submitted by INES ARAVENA

FDA 510(k) Number Submission Date Device Name Applicant
K130572 03/04/2013 INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM IMPLANT DIRECT SYBRON MANUFACTURING LLC
K131097 04/18/2013 LEGACY3 6MM LENGTH IMPLANTS IMPLANT DIRECT SYBRON MANUFACTURING LLC


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