FDA 510(k) Application Details - K093897

Device Classification Name	Fastener, Fixation, Nondegradable, Soft Tissue   More FDA Info for this Device
510(K) Number	K093897
Device Name	Fastener, Fixation, Nondegradable, Soft Tissue
Applicant	SMITH & NEPHEW INC., ENDOSCOPY DIV. 150 MINUTEMAN RD. ANDOVER, MA 01810 US Other 510(k) Applications for this Company
Contact	CHRISTINA FLORES Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	MBI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/18/2009
Decision Date	03/04/2010
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