FDA 510(k) Application Details - K011087

Device Classification Name	Syringe, Piston   More FDA Info for this Device
510(K) Number	K011087
Device Name	Syringe, Piston
Applicant	ORTHOVITA, INC. 45 GREAT VALLEY PKWY. MALVERN, PA 19355 US Other 510(k) Applications for this Company
Contact	ANGIE IDE Other 510(k) Applications for this Contact
Regulation Number	880.5860   More FDA Info for this Regulation Number
Classification Product Code	FMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/10/2001
Decision Date	09/19/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review