PDO Max Suture with Dual Needle
K号: K210871 · 2021-12-17
广告
器械摘要
PDO Max Suture with Dual Needle is the device name listed in this FDA 510(k) record. The listed applicant is Pdo Max, Inc.. It received FDA 510(k) clearance on 2021-12-17 under 510(k) number K210871. 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 PDO Max Suture with Dual Needle?
PDO Max Suture with Dual Needle is a medical device that received FDA 510(k) clearance on 2021-12-17. The listed applicant is Pdo Max, Inc.. The 510(k) number is K210871.
When did PDO Max Suture with Dual Needle receive FDA 510(k) clearance?
PDO Max Suture with Dual Needle received FDA 510(k) clearance on 2021-12-17, under 510(k) number K210871.
Who is the listed applicant for PDO Max Suture with Dual Needle?
The FDA 510(k) record lists Pdo Max, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PDO Max Suture with Dual Needle?
The FDA product code for PDO Max Suture with Dual Needle 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。
列明Pdo Max, 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。
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, LLCK252171倒刺 PDO 缝线Sutura Medical Technology, Inc.K252047STRATAFIX® 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.
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。
广告