FDA 510(k) Application Details - K091432

Device Classification Name	Suture, Nonabsorbable, Synthetic, Polyethylene   More FDA Info for this Device
510(K) Number	K091432
Device Name	Suture, Nonabsorbable, Synthetic, Polyethylene
Applicant	ANULEX TECHNOLOGIES, INC 5600 ROWLAND ROAD, STE 280 MINNETONKA, MN 55343 US Other 510(k) Applications for this Company
Contact	RACHEL KENNEDY Other 510(k) Applications for this Contact
Regulation Number	878.5000   More FDA Info for this Regulation Number
Classification Product Code	GAT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/14/2009
Decision Date	06/12/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review