倒刺 PDO 缝线
K号: K252171 · 2026-06-12
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决定日期2026-06-12
产品代码NEW
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
Barbed PDO Suture is the device name listed in this FDA 510(k) record. The listed applicant is Sutura Medical Technology, Inc.. It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K252171. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Barbed PDO Suture?
Barbed PDO Suture is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Sutura Medical Technology, Inc.. The 510(k) number is K252171.
When did Barbed PDO Suture receive FDA 510(k) clearance?
Barbed PDO Suture received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252171.
Who is the listed applicant for Barbed PDO Suture?
The FDA 510(k) record lists Sutura Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Barbed PDO Suture?
The FDA product code for Barbed PDO Suture is NEW.
相关临床试验
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。
相关器械（代码：NEW）
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。
K254238MINT MONO 缝线Hans Biomed CorporationK253879单固定PDOSamyang Holdings CorporationK261988Monodek® (POLYDIOXANONE) 染成紫罗兰色的单丝合成可吸收外科缝合线Teleflex Medical, LLCK252047STRATAFIX® 对称 PDS® Plus 无结组织控制装置ETHICON, Inc.K243897PDS™ Plus 抗菌 (聚二氧杂环己酮) 灭菌合成可吸收外科缝合线ETHICON, Inc.K251414Miracu™ 聚二氧杂环己酮 (PDO) 缝线和针 (MONO)Feeltech Co., Ltd.
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。
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