DURAMESH 网状缝合线
K号: K211178 · 2022-09-02
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器械摘要
DURAMESH Mesh Suture is the device name listed in this FDA 510(k) record. The listed applicant is Msi. It received FDA 510(k) clearance on 2022-09-02 under 510(k) number K211178. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DURAMESH Mesh Suture?
DURAMESH Mesh Suture is a medical device that received FDA 510(k) clearance on 2022-09-02. The listed applicant is Msi. The 510(k) number is K211178.
When did DURAMESH Mesh Suture receive FDA 510(k) clearance?
DURAMESH Mesh Suture received FDA 510(k) clearance on 2022-09-02, under 510(k) number K211178.
Who is the listed applicant for DURAMESH Mesh Suture?
The FDA 510(k) record lists Msi as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DURAMESH Mesh Suture?
The FDA product code for DURAMESH Mesh Suture is GAW.
相关临床试验
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相关器械（代码：GAW）
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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