FDA 510(k) Application Details - K082518

Device Classification Name	Suture, Nonabsorbable, Synthetic, Polyethylene   More FDA Info for this Device
510(K) Number	K082518
Device Name	Suture, Nonabsorbable, Synthetic, Polyethylene
Applicant	CAYENNE MEDICAL, INC. 16597 N. 92ND STREET SUITE 101 SCOTTSDALE, AZ 85260 US Other 510(k) Applications for this Company
Contact	KERESHMEH SHAHRIARI 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	09/02/2008
Decision Date	01/16/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review