NET品牌骨钉固定系统
K号: K233150 · 2024-02-20
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决定日期2024-02-20
产品代码JDS
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：
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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]
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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
NET BRAND Osteosynthesis Nailing System is the device name listed in this FDA 510(k) record. The listed applicant is Narang Medical , Ltd.. It received FDA 510(k) clearance on 2024-02-20 under 510(k) number K233150. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NET BRAND Osteosynthesis Nailing System?
NET BRAND Osteosynthesis Nailing System is a medical device that received FDA 510(k) clearance on 2024-02-20. The listed applicant is Narang Medical , Ltd.. The 510(k) number is K233150.
When did NET BRAND Osteosynthesis Nailing System receive FDA 510(k) clearance?
NET BRAND Osteosynthesis Nailing System received FDA 510(k) clearance on 2024-02-20, under 510(k) number K233150.
Who is the listed applicant for NET BRAND Osteosynthesis Nailing System?
The FDA 510(k) record lists Narang Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NET BRAND Osteosynthesis Nailing System?
The FDA product code for NET BRAND Osteosynthesis Nailing System is JDS.
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：JDS）
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。
K243608TRIGEN 稳定锁紧螺母与垫圈Smith & Nephew, Inc.K240061TRIGEN MAX 胫骨钉系统；INTERTAN MAX 髋部骨折钉系统Smith & Nephew, Inc.K241804TRIGEN INTERTAN 10S 钉系统Smith & Nephew, Inc.K230761TRIGEN META-NAIL 钉系统Smith & Nephew, Inc.K201336DePuy Synthes 股骨远端钉高级，DePuy Synthes 骨髓钉锁定螺钉，4.0 和 5.0 毫米Synthes (USA) Products, LLCK192003Auxein 钉系统Auxein Medical Private Limited
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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