OsteoMed ExtremiFix 微型和小型穿刺螺钉系统
K号: K202680 · 2020-10-15
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器械摘要
常见问题
What is the OsteoMed ExtremiFix Mini & Small Cannulated Screw System?
OsteoMed ExtremiFix Mini & Small Cannulated Screw System is a medical device that received FDA 510(k) clearance on 2020-10-15. The listed applicant is Osteomed, LLC. The 510(k) number is K202680.
When did OsteoMed ExtremiFix Mini & Small Cannulated Screw System receive FDA 510(k) clearance?
OsteoMed ExtremiFix Mini & Small Cannulated Screw System received FDA 510(k) clearance on 2020-10-15, under 510(k) number K202680.
Who is the listed applicant for OsteoMed ExtremiFix Mini & Small Cannulated Screw System?
The FDA 510(k) record lists Osteomed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OsteoMed ExtremiFix Mini & Small Cannulated Screw System?
The FDA product code for OsteoMed ExtremiFix Mini & Small Cannulated Screw System is HWC. This falls under the Cardiovascular category.
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Osteomed, LLC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:HWC)
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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