K&J IVA(ACIF,DLIF,PLIF,TLIF,ALIF)PEEK笼
K号: K212038 · 2021-08-27
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器械摘要
常见问题
What is the K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage?
K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage is a medical device that received FDA 510(k) clearance on 2021-08-27. The listed applicant is K&J Consulting Corporation. The 510(k) number is K212038.
When did K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage receive FDA 510(k) clearance?
K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage received FDA 510(k) clearance on 2021-08-27, under 510(k) number K212038.
Who is the listed applicant for K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage?
The FDA 510(k) record lists K&J Consulting Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage?
The FDA product code for K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage is ODP.
列明K&J Consulting Corporation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:ODP)
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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