Kyphon, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Kyphon, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 9 cleared submissions from 1998 to 2008. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kyphon, Inc. Filter by specialty or product code using the sidebar.
9 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
Cleared
Jul 09, 2004
KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13A
Orthopedic
38d
Cleared
Jul 07, 2004
KYPHX HV-R BONE CEMENT, MODEL C01A
Orthopedic
23d
Cleared
Apr 01, 2004
KYPHX HV-R, MODEL C01A
Orthopedic
115d
Cleared
Sep 15, 2003
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
Orthopedic
56d
Cleared
Feb 14, 2001
KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP,...
Orthopedic
19d
Cleared
Jul 02, 1998
KYPHON INFLATABLE BONE TAMP
Orthopedic
87d