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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Neurovascular Embolization
510(k) Number K200030
Device Name Optima Coil System
Applicant
Balt USA, LLC
29, Parker
Irvine,  CA  92618
Applicant Contact Michael Peters
Correspondent
Balt USA, LLC
29, Parker
Irvine,  CA  92618
Correspondent Contact Michael Peters
Regulation Number882.5950
Classification Product Code
HCG  
Subsequent Product Code
KRD  
Date Received01/07/2020
Decision Date 02/01/2020
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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