FDA 510(k) Application Details - K061925

Device Classification Name	Washer, Bolt Nut   More FDA Info for this Device
510(K) Number	K061925
Device Name	Washer, Bolt Nut
Applicant	ARTHREX, INC. 1370 CREEKSIDE BLVD. NAPLES, FL 34108-1945 US Other 510(k) Applications for this Company
Contact	SALLY FOUST Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	HTN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/2006
Decision Date	10/31/2006
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