FDA 510(k) Application Details - K983577

Device Classification Name	Fastener, Fixation, Biodegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K983577
Device Name	Fastener, Fixation, Biodegradable, Soft Tissue
Applicant	ARTHREX, INC. 2885 SOUTH HORSESHOE DR. NAPLES, FL 34104 US Other 510(k) Applications for this Company
Contact	SCOTT M DURLACHER 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	10/13/1998
Decision Date	08/13/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review