Altiva Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Altiva Corp. has 5 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Historical record: 5 cleared submissions from 2005 to 2007. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Altiva Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Jun 11, 2007
ALTIVA CLASSIC ACP SYSTEM
Orthopedic
73d
Cleared
Jul 26, 2006
ALTES BUTTRESS PLATING SYSTEM
Orthopedic
57d
Cleared
Feb 13, 2006
CONTOUR II SPINAL SYSTEM
Orthopedic
104d
Cleared
Oct 07, 2005
ARCTEC SEMIRIGID PLATING SYSTEM
Orthopedic
165d
Cleared
Jul 19, 2005
HYDRALOK SYSTEM
Orthopedic
68d