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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name platelet and plasma separator for bone graft handling
510(k) Number BK120048
Tradename Intra-Spin System
Device Name Platelet And Plasma Separator For Bone Graft Handling
Original Applicant
Intra-Lock International
6560 west rogers circle
boca raton,  FL  33487
Regulation Number864.9245
Classification Product Code
ORG  
Date Received08/17/2012
Decision Date 01/28/2013
Decision substantially equivalent (SE)
Classification Advisory Committee Hematology
Review Advisory Committee Hematology
Type 510(k) Traditional
Total Product Life Cycle (TPLC) TPLC Device Report
Reviewed by Third Party No
Expedited Review No
Combination Product No
In Vitro Product No
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