Mastergraft Matrix EXT;Mastergraft 条带;Mastergraft Putty;Mastergraft 粒状物
K号: K243706 · 2025-01-17
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器械摘要
常见问题
What is the Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?
Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is a medical device that received FDA 510(k) clearance on 2025-01-17. The listed applicant is Medtronic Sofamor Danek, Inc.. The 510(k) number is K243706.
When did Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules receive FDA 510(k) clearance?
Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules received FDA 510(k) clearance on 2025-01-17, under 510(k) number K243706.
Who is the listed applicant for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?
The FDA 510(k) record lists Medtronic Sofamor Danek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules?
The FDA product code for Mastergraft Matrix EXT; Mastergraft Strip; Mastergraft Putty; Mastergraft Granules is MQV.
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。
列明Medtronic Sofamor Danek, Inc.为申报人的其他记录
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:MQV)
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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