异种移植牛骨颗粒
K号: K240133 · 2024-08-16
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决定日期2024-08-16
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
Xenograft Bovine Bone Particulate is the device name listed in this FDA 510(k) record. The listed applicant is Collagen Solutions, LLC. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K240133. 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 Xenograft Bovine Bone Particulate?
Xenograft Bovine Bone Particulate is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is Collagen Solutions, LLC. The 510(k) number is K240133.
When did Xenograft Bovine Bone Particulate receive FDA 510(k) clearance?
Xenograft Bovine Bone Particulate received FDA 510(k) clearance on 2024-08-16, under 510(k) number K240133.
Who is the listed applicant for Xenograft Bovine Bone Particulate?
The FDA 510(k) record lists Collagen Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Xenograft Bovine Bone Particulate?
The FDA product code for Xenograft Bovine Bone Particulate is NPM.
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：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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