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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 BK251196
Tradename Exocube Set
Device Name Platelet And Plasma Separator For Bone Graft Handling
Original Applicant
StemC Biyoteknoloji Anonim Sirketi
stemc biyoteknoloji anonim sirketi
b:2 blok iç kapi no:27 kagithane
istanbul,  Istanbul,  34406,  TURKEY
Regulation Number864.9245
Classification Product Code
ORG  
Date Received04/21/2025
Decision Date 08/28/2025
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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