OOD
- 产品代码
- OOD
- 器械名称
- Surgical Film
- 管理类别
- 第 2 类(Class II)
- 21 CFR 条款
- 21 CFR 878.3300
- FDA 专业组
- General, Plastic Surgery
- 上市路径
- 需提交 510(k) 上市前通告
- 标记
- 属植入器械
- 标记
- 属生命支持/维持器械
- 该代码近三年的 510(k)
- 1 件
- 其中 Summary 已存档
- 1 份,可直接下载
- FDA 历史累计 510(k)
- 13 件(全部年份;本站只收录近三年的明细)
FDA 分类定义
To be implanted to reinforce soft tissue or bone where weakness exists. Intended to be used wherever temporary wound support is required, to reinforce soft tissues where weakness exists in the urological, gynecological, or gastrointestinal anatomy, or for the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result. The absorbable protective film also may help minimize the potential for tissue attachment to the device in case of direct contact with the viscera.
该代码近三年的 510(k)(1 件)
| 510(k) 号 | 批准日期 | 申请人 | 器械名称 | 摘要 |
|---|---|---|---|---|
| K233999 | 2024-04-09 | Tepha, Inc. | GalaFLEX LITE Scaffold |
FDA 官方分类页: OOD
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。