FDA 510(k)

Biodesign 瘘管塞

K号: K170016 · 2017-06-21

决定日期2017-06-21

产品代码FTM

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决定实质等同

器械摘要

Biodesign Fistula Plug is the device name listed in this FDA 510(k) record. The listed applicant is Cook Biotech Incorporated. It received FDA 510(k) clearance on 2017-06-21 under 510(k) number K170016. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Biodesign Fistula Plug?

Biodesign Fistula Plug is a medical device that received FDA 510(k) clearance on 2017-06-21. The listed applicant is Cook Biotech Incorporated. The 510(k) number is K170016.

When did Biodesign Fistula Plug receive FDA 510(k) clearance?

Biodesign Fistula Plug received FDA 510(k) clearance on 2017-06-21, under 510(k) number K170016.

Who is the listed applicant for Biodesign Fistula Plug?

The FDA 510(k) record lists Cook Biotech Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Biodesign Fistula Plug?

The FDA product code for Biodesign Fistula Plug is FTM.

列明Cook Biotech Incorporated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。

K232646Biodesign 耳科蝴蝶移植（ENT-OTO-BFLY-0.4-0.6）；Biodesign 耳科蝴蝶移植（ENT-OTO-BFLY-0.6-0.9）K201000Biodesign 线圈加固 K191696Biodesign 肛门瘘管塞，Biodesign 瘘管塞，Biodesign 整形外科基质，Biodesign 组织移植 K171817Biodesign 膈肌裂孔移植 K162934Biodesign 肠造口旁疝修复移植 K170945Biodesign 线圈加固

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官方来源

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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。