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Kyphon, Inc.

9 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR (K073516)Kyphon, Inc.2008-02-21
DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B (K063071)Kyphon, Inc.2007-04-13
FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01B (K061210)Kyphon, Inc.2006-06-27
KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13A (K041454)Kyphon, Inc.2004-07-09
KYPHX HV-R BONE CEMENT, MODEL C01A (K041584)Kyphon, Inc.2004-07-07
KYPHX HV-R, MODEL C01A (K033801)Kyphon, Inc.2004-04-01
KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A (K032212)Kyphon, Inc.2003-09-15
KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP, SIZE 15/3, MODEL K02A (K010246)Kyphon, Inc.2001-02-14
KYPHON INFLATABLE BONE TAMP (K981251)Kyphon, Inc.1998-07-02

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Every clearance here is in the API, with alerts when new ones post.