FDA 510(k)

Stryker MP，下颌骨，HMMF 和 MMF AXS 螺丝

K号: K231599 · 2023-08-24

决定日期2023-08-24

产品代码DZL

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决定实质等同

器械摘要

Stryker MP, Mandible, HMMF and MMF AXS Screws is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2023-08-24 under 510(k) number K231599. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Stryker MP, Mandible, HMMF and MMF AXS Screws?

Stryker MP, Mandible, HMMF and MMF AXS Screws is a medical device that received FDA 510(k) clearance on 2023-08-24. The listed applicant is Stryker Leibinger GmbH & Co KG. The 510(k) number is K231599.

When did Stryker MP, Mandible, HMMF and MMF AXS Screws receive FDA 510(k) clearance?

Stryker MP, Mandible, HMMF and MMF AXS Screws received FDA 510(k) clearance on 2023-08-24, under 510(k) number K231599.

Who is the listed applicant for Stryker MP, Mandible, HMMF and MMF AXS Screws?

The FDA 510(k) record lists Stryker Leibinger GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stryker MP, Mandible, HMMF and MMF AXS Screws?

The FDA product code for Stryker MP, Mandible, HMMF and MMF AXS Screws is DZL.

列明Stryker Leibinger GmbH & Co KG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。

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官方来源

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