FDA 510(k)

BioPoly 大脚趾半关节置换植入物

K号: K203634 · 2021-02-02

决定日期2021-02-02

产品代码KWD

咨询委员会OR 请注意，由于原文中未提供具体的医疗设备监管文本，以下是一个示例翻译，您可以根据实际文本进行调整： --- 产品名称：[产品名称] 公司名称：[公司名称] 根据FDA 510(k)预市场批准程序，[产品名称]已获得批准，用于[产品用途描述]。产品注册号：[注册号] PMA编号：[PMA编号] 临床试验编号（NCT）：[NCT编号] PubMed ID（PMID）：[PMID编号] 更多信息请访问以下链接： [URL] --- 请将上述示例中的[产品名称]、[公司名称]、[注册号]、[PMA编号]、[NCT编号]、[PMID编号]和[URL]替换为实际的文本内容。

决定实质等同

器械摘要

BioPoly Great Toe Hemiarthroplasty Implant is the device name listed in this FDA 510(k) record. The listed applicant is BioPoly, LLC. It received FDA 510(k) clearance on 2021-02-02 under 510(k) number K203634. The device is classified under product code KWD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BioPoly Great Toe Hemiarthroplasty Implant?

BioPoly Great Toe Hemiarthroplasty Implant is a medical device that received FDA 510(k) clearance on 2021-02-02. The listed applicant is BioPoly, LLC. The 510(k) number is K203634.

When did BioPoly Great Toe Hemiarthroplasty Implant receive FDA 510(k) clearance?

BioPoly Great Toe Hemiarthroplasty Implant received FDA 510(k) clearance on 2021-02-02, under 510(k) number K203634.

Who is the listed applicant for BioPoly Great Toe Hemiarthroplasty Implant?

The FDA 510(k) record lists BioPoly, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BioPoly Great Toe Hemiarthroplasty Implant?

The FDA product code for BioPoly Great Toe Hemiarthroplasty Implant is KWD.

列明BioPoly, LLC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。

K233592BioPoly 肱骨小头植入物 K222964BioPoly 小脚趾半关节置换植入物

官方来源

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