FTL

Mesh, Surgical, Polymeric

产品代码
FTL
器械名称
Mesh, Surgical, Polymeric
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
该代码近三年的 510(k)
336 件

该代码近三年的 510(k)(11 件)

数据窗口为最近三年。最新一件:2026-05-21。

510(k) 号批准日期申请人器械名称
K2539562026-05-21Sofradim ProductionProGrip™ advanced self-gripping polypropylene mesh ( 摘要
K2531252025-10-24Medtronic - Sofradim ProductionParietene™ Flat Sheet Mesh 摘要
K2519552025-07-24Davol Inc., Subsidiary of C. R. Bard, Onflex™ Mesh 摘要
K2515572025-06-12Davol, Inc.Bard® Mesh; Bard® Mesh Pre-Shaped 摘要
K2508692025-04-23Sofradim ProductionParietene™ Macroporous Mesh (PPM5050 ) 摘要
K2500982025-04-09Davol, Inc.Bard Soft Mesh; Bard Soft Mesh Pre-Shaped 摘要
K2433152025-01-17Sofradim ProductionProGrip™ Self-Gripping Polypropylene Mesh 摘要
K2412502024-06-14Davol Inc., Subsidiary of C. R. Bard, 3DMax Light Mesh 摘要
K2323732024-01-18Sofradim ProductionProgrip™ Self-Gripping Polypropylene Mesh 摘要
K2334022023-11-01Davol Inc., Subsidiary of C. R. Bard, Bard 3DMax Mesh 摘要
K2329242023-10-18Deep Blue Medical Advances, Inc.T-Line® Hernia Mesh 摘要
FDA 官方分类页: FTL
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。