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FDA 510(k)

Smith & Nephew, Inc. 板和螺钉系统：EVOS，Peri-Loc，D-Rad，TC-100，VLP Mini-Mod，压缩髋螺钉（CHS），CONQUEST FN 和空心螺钉

K号: K213126 · 2022-09-29

申请人Smith & Nephew, Inc.
决定日期2022-09-29
产品代码JDO
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

Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2022-09-29 under 510(k) number K213126. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws?

Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws is a medical device that received FDA 510(k) clearance on 2022-09-29. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K213126.

When did Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws receive FDA 510(k) clearance?

Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws received FDA 510(k) clearance on 2022-09-29, under 510(k) number K213126.

Who is the listed applicant for Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws?

FDA 510(k)记录中列出Smith & Nephew, Inc.为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws?

The FDA product code for Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screws is JDO.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Smith & Nephew, 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。

K261462LANDMARK 全膝关节系统K261968Q-FIX KNOTLESS 全缝合锚，2.8mm，带一个黑色无结和一根蓝色 MINITAPE 缝线（72205981）；Q-FIX KNOTLESS 全缝合锚，2.8mm，带一个蓝色无结和一根黑色 MINITAPE 缝线（72205982）K254084AETOS ǽ - CONCELOC GlenoidsK252416AETOS ǽ Meta ʽK252129AETOS ǽ ʽK251627BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (编织蓝色)；BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (编织黑色)；BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (白色)；BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (编织黑色)；BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (编织蓝色)

查看所有 112 个设备 →

相关器械（代码：JDO）

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。

K230764OsteoCentric 集成髋关节固定器系统OsteoCentric TechnologiesK210247OsteoCentric 集成髋关节固定器系统Osteocentric Technologies D.B.A. Osteocentric TraumaK193029CONQUEST FNSmith & Nephew, Inc.K173826THP髋部骨折钢板系统Biomet, Inc.K172785CONQUEST FNSmith & NephewK152686CONQUEST FNSmith & Nephew

官方来源

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