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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Fastener, Fixation, Nondegradable, Soft Tissue
510(k) Number K240213
Device Name Iconix Knotless Anchor
Applicant
Riverpoint Medical
825 NE 25th Avenue
Portland,  OR  97232
Applicant Contact Bianca Silva de Sousa
Correspondent
Riverpoint Medical
825 NE 25th Avenue
Portland,  OR  97232
Correspondent Contact Bianca Silva de Sousa
Regulation Number888.3040
Classification Product Code
MBI  
Date Received01/25/2024
Decision Date 02/23/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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