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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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