Blustone Synergy 腰椎椎间融合系统(玄武岩,岩浆,辉石),Blustone Synergy 颈椎椎间融合系统(板岩)
K号: K171893 · 2017-09-08
广告
器械摘要
常见问题
What is the Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)?
Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate) is a medical device that received FDA 510(k) clearance on 2017-09-08. The listed applicant is Bluestone Synergy. The 510(k) number is K171893.
When did Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate) receive FDA 510(k) clearance?
Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate) received FDA 510(k) clearance on 2017-09-08, under 510(k) number K171893.
Who is the listed applicant for Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)?
The FDA 510(k) record lists Bluestone Synergy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate)?
The FDA product code for Blustone Synergy Lumbar Interbody Fusion System (Basalt, Magma, Obsidian), Blustone Synergy Cervical Interbody Fusion System (Slate) is MAX.
相关临床试验
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:MAX)
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。
广告