Medical Device Manufacturer · US , Sunnyvale , CA

Kyphon, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1998

Recent clearances: DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR, DISCYPHOR CATHETER SYSTEM, MODEL D01A, FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A

View 9 510(k) Devices ↓

9

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kyphon, Inc. Anesthesiology ✕

3 devices

1-3 of 3

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