InterOss 胶原蛋白
K号: K221808 · 2023-03-18
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决定日期2023-03-18
产品代码NPM
咨询委员会DE
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决定实质等同
器械摘要
InterOss Collagen is the device name listed in this FDA 510(k) record. The listed applicant is Sigmagraft, Inc.. It received FDA 510(k) clearance on 2023-03-18 under 510(k) number K221808. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the InterOss Collagen?
InterOss Collagen is a medical device that received FDA 510(k) clearance on 2023-03-18. The listed applicant is Sigmagraft, Inc.. The 510(k) number is K221808.
When did InterOss Collagen receive FDA 510(k) clearance?
InterOss Collagen received FDA 510(k) clearance on 2023-03-18, under 510(k) number K221808.
Who is the listed applicant for InterOss Collagen?
The FDA 510(k) record lists Sigmagraft, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InterOss Collagen?
The FDA product code for InterOss Collagen is NPM.
相关临床试验
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列明Sigmagraft, 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：NPM）
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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