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  1. Substantially Equivalent 510(k) Device Information

BK210655 - Arthrex Autologous Conditioned Plasma (ACP) Max PRP System

510(k) Number: BK210655
Applicant: Arthrex, Inc.
Device Name: Arthrex Autologous Conditioned Plasma (ACP) Max™ PRP System
Decision Date: 9/22/2022

Supporting Documents

 
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