MEH

Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

产品代码
MEH
器械名称
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 888.3353
FDA 专业组
Orthopedic
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)
160 件

该代码近三年的 510(k)(12 件)

数据窗口为最近三年。最新一件:2026-08-10。

510(k) 号批准日期申请人器械名称
K2615762026-08-10Corin, Ltd.Icona Hip Stem 摘要
K2503752025-11-05Waldemar Link GmbH & Co. KGAllure Hip Stem and Intramedullary Plugs 摘要
K2511662025-06-13Medacta International S.A.Mfinity Femoral System 摘要
K2510522025-05-22Ortho Development Corp.Trivicta® Hip Stem 摘要
K2423152025-05-01United Orthopedic CorporationResolve Modular Revision Hip Stem 摘要
K2438392025-03-10Exactech, Inc.Alteon® HA Femoral Stems 摘要
K2431622024-11-25Signature Orthopaedics Pty, Ltd.World Liner 摘要
K2414722024-10-03Corin U.S.A. LimitedIcona Hip Stem 摘要
K2418752024-09-13Nextstep ArthropedixTheRay Collared and Collarless Femoral Stem 摘要
K2416902024-08-01Signature Orthopaedics Pty, Ltd.Logical Liner; World Liner; World Knee Patella 摘要
K2337582024-03-08Ortho Development Corp.Trivicta™ Hip Stem 摘要
K2318732024-01-19Depuy Ireland UCDePuy SUMMIT Porocoat Hip Prosthesis – MR Conditiona 摘要
FDA 官方分类页: MEH
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。