FDA 510(k)

TELIGEN 系统导航就绪指示（TELIGEN 访问探头，TELIGEN 清晰）

K号: K223108 · 2023-01-19

决定日期2023-01-19

产品代码OLO

咨询委员会NE 请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2023-01-19 under 510(k) number K223108. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear)?

TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) is a medical device that received FDA 510(k) clearance on 2023-01-19. The listed applicant is Medos International SARL. The 510(k) number is K223108.

When did TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) receive FDA 510(k) clearance?

TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) received FDA 510(k) clearance on 2023-01-19, under 510(k) number K223108.

Who is the listed applicant for TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear)?

The FDA 510(k) record lists Medos International SARL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear)?

The FDA product code for TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) is OLO.

列明Medos International SARL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。

K254157CROSSNAV 导航启用工具用于椎间盘准备和椎间 K260240SYMPHONY Navigation Ready Instruments K253249TriALTIS™ 脊柱系统 K243249TriALTIS™ 脊柱系统 K241893CROSSNAV 导航启用工具和UNAS 导航阵列 K242042TriALTIS™ 脊柱系统

查看所有 75 个设备 →

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。