Kyphon, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
3 devices
Cleared
Feb 21, 2008
DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR...
Anesthesiology
69d
Cleared
Apr 13, 2007
DISCYPHOR CATHETER SYSTEM, MODEL D01A
Anesthesiology
189d
Cleared
Jun 27, 2006
FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A
Anesthesiology
57d