Ortho Aligner System
K号: K212496 · 2021-11-04
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决定日期2021-11-04
产品代码NXC
咨询委员会DE
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决定实质等同
器械摘要
Ortho Aligner System is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Lab Services, LLC. It received FDA 510(k) clearance on 2021-11-04 under 510(k) number K212496. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Ortho Aligner System?
Ortho Aligner System is a medical device that received FDA 510(k) clearance on 2021-11-04. The listed applicant is Ortho Lab Services, LLC. The 510(k) number is K212496.
When did Ortho Aligner System receive FDA 510(k) clearance?
Ortho Aligner System received FDA 510(k) clearance on 2021-11-04, under 510(k) number K212496.
Who is the listed applicant for Ortho Aligner System?
The FDA 510(k) record lists Ortho Lab Services, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ortho Aligner System?
The FDA product code for Ortho Aligner System is NXC.
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相关器械（代码：NXC）
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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