Kyphon, Inc.
FDA 510(k) medical device clearances.
Top product codes for Kyphon, Inc.
Recent clearances by Kyphon, Inc.
- K073516 — DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR
- K063071 — DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B
- K061210 — FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01B
- K041454 — KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13A
- K041584 — KYPHX HV-R BONE CEMENT, MODEL C01A
- K033801 — KYPHX HV-R, MODEL C01A
- K032212 — KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
- K010246 — KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP, SIZE 15/3, MODEL K02A
- K981251 — KYPHON INFLATABLE BONE TAMP
Data sourced from openFDA. This site is unofficial and independent of the FDA.