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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Syringe, Piston
510(k) Number K022246
Device Name MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM
Applicant
Depuyacromed
325 Paramount Dr.
Raynham,  MA  02767 -0350
Applicant Contact KAREN F JURCZAK
Correspondent
Depuyacromed
325 Paramount Dr.
Raynham,  MA  02767 -0350
Correspondent Contact KAREN F JURCZAK
Regulation Number880.5860
Classification Product Code
FMF  
Date Received07/12/2002
Decision Date 08/02/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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