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Kyphon, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K073516 DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULARBSP2008-02-21 View
510(k) K063071 DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01BBSP2007-04-13 View
510(k) K061210 FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01BBSP2006-06-27 View
510(k) K041454 KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13AHRX2004-07-09 View
510(k) K041584 KYPHX HV-R BONE CEMENT, MODEL C01ANDN2004-07-07 View
510(k) K033801 KYPHX HV-R, MODEL C01ANDN2004-04-01 View
510(k) K032212 KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17AHRX2003-09-15 View
510(k) K010246 KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP, SIZE 15/3, MODEL K02AHRX2001-02-14 View
510(k) K981251 KYPHON INFLATABLE BONE TAMPHRX1998-07-02 View
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