Kyphon, Inc.
9 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| 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.