PPN
- 产品代码
- PPN
- 器械名称
- Percutaneous Catheter, Ultrasound
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 870.1250
- FDA 专业组
- Cardiovascular
- 上市路径
- 需提交 510(k) 上市前通告
- 该代码近三年的 510(k)
- 14 件
FDA 分类定义
Intended for ultrasound wave enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature.
该代码近三年的 510(k)(6 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K260246 | 2026-08-24 | Bolt Medical, Inc. | SEISMIQ Intravascular Lithotripsy System | |
| K262201 | 2026-07-27 | Shockwave Medical, Inc. | Shockwave Intravascular Lithotripsy (IVL) System wit | |
| K250225 | 2025-03-25 | Bolt Medical, Inc. | Bolt Intravascular Lithotripsy (IVL) System | |
| K242213 | 2024-09-27 | Shockwave Medical, Inc. | Shockwave Intravascular Lithotripsy (IVL) System wit | |
| K240954 | 2024-05-07 | Shockwave Medical, Inc. | Shockwave Intravascular Lithotripsy (IVL) System wit | |
| K240225 | 2024-03-22 | Shockwave Medical, Inc. | Shockwave Intravascular Lithotripsy (IVL) System wit |
FDA 官方分类页: PPN
分类与上市路径以 FDA 现行公告为准。本页数据来自 openFDA(CC0 公有领域),不构成注册策略建议。