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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
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