FDA 510(k)

Asnis® III 套管螺丝系统及 Asnis® PRO 套管螺丝系统

K号: K213199 · 2022-01-11

决定日期2022-01-11

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

Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker GmbH. It received FDA 510(k) clearance on 2022-01-11 under 510(k) number K213199. 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 Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System?

Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System is a medical device that received FDA 510(k) clearance on 2022-01-11. The listed applicant is Stryker GmbH. The 510(k) number is K213199.

When did Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System receive FDA 510(k) clearance?

Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System received FDA 510(k) clearance on 2022-01-11, under 510(k) number K213199.

Who is the listed applicant for Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System?

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

What is the FDA product code for Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System?

The FDA product code for Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System is HWC. This falls under the Cardiovascular category.

列明Stryker GmbH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。

K261481Pangea股骨重建系统 K253640T2 Alpha股骨逆行固定系统；Pangea股骨重建系统 K253202Hoffmann LRF 系统 K251400T2 Alpha肱骨内固定系统；IMN螺钉系统；T2内固定系统 K250163T2 Alpha股骨逆行固定系统 K242445Pangea平台；Pangea股骨接骨板系统；Pangea肱骨接骨板系统；Pangea胫骨接骨板系统

查看所有 53 个设备 →

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。