FDA 510(k)

DePuy Synthes 2.0 mm 快速插入螺钉

K号: K180541 · 2018-11-21

决定日期2018-11-21

产品代码HWC

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

DePuy Synthes 2.0 mm Quick Insertion Screws is the device name listed in this FDA 510(k) record. The listed applicant is Synthes USA Products, LLC. It received FDA 510(k) clearance on 2018-11-21 under 510(k) number K180541. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常见问题

What is the DePuy Synthes 2.0 mm Quick Insertion Screws?

DePuy Synthes 2.0 mm Quick Insertion Screws is a medical device that received FDA 510(k) clearance on 2018-11-21. The listed applicant is Synthes USA Products, LLC. The 510(k) number is K180541.

When did DePuy Synthes 2.0 mm Quick Insertion Screws receive FDA 510(k) clearance?

DePuy Synthes 2.0 mm Quick Insertion Screws received FDA 510(k) clearance on 2018-11-21, under 510(k) number K180541.

Who is the listed applicant for DePuy Synthes 2.0 mm Quick Insertion Screws?

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

What is the FDA product code for DePuy Synthes 2.0 mm Quick Insertion Screws?

The FDA product code for DePuy Synthes 2.0 mm Quick Insertion Screws is HWC. This falls under the Cardiovascular category.

列明Synthes USA Products, 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。

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