FDA 510(k) Application Details - K050795

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K050795
Device Name	Instrument, Biopsy
Applicant	ORTHOVITA, INC. 1835 MARKET ST. 28TH FLOOR PHILADELPHIA, PA 19103 US Other 510(k) Applications for this Company
Contact	JANICE M HOGAN Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/29/2005
Decision Date	06/03/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review