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FDA 510(k)

Pounce XL Thrombectomy System (PTS-1011-7F135)

K号: K241362 · 2024-09-11

决定日期2024-09-11
产品代码QEW
咨询委员会CV 请注意,由于原文未提供具体内容,以下是一个示例翻译: --- 产品名称:[产品名称] 公司名称:[公司名称] FDA批准号:[FDA批准号] 510(k)申请号:[510(k)申请号] PMA申请号:[PMA申请号] 临床试验注册号:[NCT] PubMed ID:[PMID] 产品标识符:[标识符] 产品URL:[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。
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器械摘要

Pounce XL Thrombectomy System (PTS-1011-7F135) is the device name listed in this FDA 510(k) record. The listed applicant is Surmodics,Inc.. It received FDA 510(k) clearance on 2024-09-11 under 510(k) number K241362. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pounce XL Thrombectomy System (PTS-1011-7F135)?

Pounce XL Thrombectomy System (PTS-1011-7F135) is a medical device that received FDA 510(k) clearance on 2024-09-11. The listed applicant is Surmodics,Inc.. The 510(k) number is K241362.

When did Pounce XL Thrombectomy System (PTS-1011-7F135) receive FDA 510(k) clearance?

Pounce XL Thrombectomy System (PTS-1011-7F135) received FDA 510(k) clearance on 2024-09-11, under 510(k) number K241362.

Who is the listed applicant for Pounce XL Thrombectomy System (PTS-1011-7F135)?

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

What is the FDA product code for Pounce XL Thrombectomy System (PTS-1011-7F135)?

The FDA product code for Pounce XL Thrombectomy System (PTS-1011-7F135) is QEW.

相关临床试验

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列明Surmodics,Inc.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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相关器械(代码:QEW)

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。

官方来源

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