scaffolene CL100 生物可吸收胶原蛋白基质
K号: K192346 · 2020-02-28
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器械摘要
scaffolene CL100 Bioresorbable Collagen Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Freudenberg Technology Innovation SE & Co. KG. It received FDA 510(k) clearance on 2020-02-28 under 510(k) number K192346. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.
常见问题
What is the scaffolene CL100 Bioresorbable Collagen Matrix?
scaffolene CL100 Bioresorbable Collagen Matrix is a medical device that received FDA 510(k) clearance on 2020-02-28. The listed applicant is Freudenberg Technology Innovation SE & Co. KG. The 510(k) number is K192346.
When did scaffolene CL100 Bioresorbable Collagen Matrix receive FDA 510(k) clearance?
scaffolene CL100 Bioresorbable Collagen Matrix received FDA 510(k) clearance on 2020-02-28, under 510(k) number K192346.
Who is the listed applicant for scaffolene CL100 Bioresorbable Collagen Matrix?
The FDA 510(k) record lists Freudenberg Technology Innovation SE & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for scaffolene CL100 Bioresorbable Collagen Matrix?
The FDA product code for scaffolene CL100 Bioresorbable Collagen Matrix is KGN.
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：KGN）
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。
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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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