FBC 921 (ALIF)
K号: K180695 · 2018-07-12
广告
决定日期2018-07-12
产品代码OVD
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：
---
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]
---
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。
决定实质等同
器械摘要
FBC 921 (ALIF) is the device name listed in this FDA 510(k) record. The listed applicant is Fbc Device Aps. It received FDA 510(k) clearance on 2018-07-12 under 510(k) number K180695. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FBC 921 (ALIF)?
FBC 921 (ALIF) is a medical device that received FDA 510(k) clearance on 2018-07-12. The listed applicant is Fbc Device Aps. The 510(k) number is K180695.
When did FBC 921 (ALIF) receive FDA 510(k) clearance?
FBC 921 (ALIF) received FDA 510(k) clearance on 2018-07-12, under 510(k) number K180695.
Who is the listed applicant for FBC 921 (ALIF)?
The FDA 510(k) record lists Fbc Device Aps as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FBC 921 (ALIF)?
The FDA product code for FBC 921 (ALIF) is OVD.
相关器械（代码：OVD）
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。
K262025Innovasis AxTiHA® 独立式 ALIF 系统；Innovasis TxTiHA® IBF 系统；Innovasis HAtetracell®-C 钛合金颈椎 IBF 系统INNO Holdings Inc. DBA InnovasisK261408SABER-XA系统Elevation SpineK261809Interwedge® 独立侧站Foundation Surgical GroupK261353Tesera-K 前路腰椎椎间融合（ALIF）系统；Tesera-K XL 系统；腰椎锚定系统Kyocera Medical Technologies, Inc.K260810Anteralign LS盖板Tyber Medical, LLCK254202MectaLIF 3D金属前部Medacta International S.A.
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。
广告