FDA 510(k) Application Details - K230435

Device Classification Name	Fastener, Fixation, Biodegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K230435
Device Name	Fastener, Fixation, Biodegradable, Soft Tissue
Applicant	Arthrex, Inc. 1370 Creekside Boulevard Naples, FL 34113 US Other 510(k) Applications for this Company
Contact	Stacy Valdez Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	MAI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/17/2023
Decision Date	03/17/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review