可吸收植入物，用于关节软骨修复
PMA编号：P210034 · 2026-06-04
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决定日期2026-06-04
PMA 编号P210034
产品代码QRU
设备分类第3类
医疗专科U
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。
器械摘要
Implant, resorbable, for articular osteochondral repair is the device name listed in this FDA 510(k) record. The listed applicant is Smith and Nephew, Inc.. It received FDA 510(k) clearance on 2026-06-04. The device is classified under product code QRU. It was reviewed by the OR advisory panel.
常见问题
What is the Implant, resorbable, for articular osteochondral repair?
Implant, resorbable, for articular osteochondral repair is a medical device that received FDA 510(k) clearance on 2026-06-04. The listed applicant is Smith and Nephew, Inc..
When did Implant, resorbable, for articular osteochondral repair receive FDA 510(k) clearance?
The clearance date for Implant, resorbable, for articular osteochondral repair can be found in the official FDA records.
Who is the listed applicant for Implant, resorbable, for articular osteochondral repair?
The FDA 510(k) record lists Smith and Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implant, resorbable, for articular osteochondral repair?
The FDA product code for Implant, resorbable, for articular osteochondral repair is QRU.
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。
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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