T2 Plus
K号: K233806 · 2024-09-06
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器械摘要
T2 Plus is the device name listed in this FDA 510(k) record. The listed applicant is Osstem Implant Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K233806. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the T2 Plus?
T2 Plus is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Osstem Implant Co., Ltd.. The 510(k) number is K233806.
When did T2 Plus receive FDA 510(k) clearance?
T2 Plus received FDA 510(k) clearance on 2024-09-06, under 510(k) number K233806.
Who is the listed applicant for T2 Plus?
The FDA 510(k) record lists Osstem Implant Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T2 Plus?
The FDA product code for T2 Plus is OAS.
列明Osstem Implant Co., Ltd.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。
相关器械（代码：OAS）
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。
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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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