FDA 510(k) Application Details - K070052

Device Classification Name	Prosthesis, Toe, Hemi-, Phalangeal   More FDA Info for this Device
510(K) Number	K070052
Device Name	Prosthesis, Toe, Hemi-, Phalangeal
Applicant	VILEX, INC. 345 OLD CURRY HOLLOW RD. PITTSBURGH, PA 15236 US Other 510(k) Applications for this Company
Contact	ABRAHAM LAVI Other 510(k) Applications for this Contact
Regulation Number	888.3730   More FDA Info for this Regulation Number
Classification Product Code	KWD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/04/2007
Decision Date	03/28/2007
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