FDA 510(k) Application Details - K965256

Device Classification Name	Dermatome   More FDA Info for this Device
510(K) Number	K965256
Device Name	Dermatome
Applicant	MATTIOLI ENGINEERING, SRL VIALE MACHIAVELLI, 2/A FLORENCE 50125 IT Other 510(k) Applications for this Company
Contact	GIAN FRANCO BERNABEI Other 510(k) Applications for this Contact
Regulation Number	878.4820   More FDA Info for this Regulation Number
Classification Product Code	GFD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/16/1996
Decision Date	12/09/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review