增材骨科患者专用3D锁定网格板
K号: K183011 · 2019-01-10
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器械摘要
常见问题
What is the Additive Orthopaedics Patient Specific 3D Locking Lattice Plates?
Additive Orthopaedics Patient Specific 3D Locking Lattice Plates is a medical device that received FDA 510(k) clearance on 2019-01-10. The listed applicant is Additive Orthopaedics. The 510(k) number is K183011.
When did Additive Orthopaedics Patient Specific 3D Locking Lattice Plates receive FDA 510(k) clearance?
Additive Orthopaedics Patient Specific 3D Locking Lattice Plates received FDA 510(k) clearance on 2019-01-10, under 510(k) number K183011.
Who is the listed applicant for Additive Orthopaedics Patient Specific 3D Locking Lattice Plates?
The FDA 510(k) record lists Additive Orthopaedics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Additive Orthopaedics Patient Specific 3D Locking Lattice Plates?
The FDA product code for Additive Orthopaedics Patient Specific 3D Locking Lattice Plates is HRS.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:HRS)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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