FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute
K号: K182670 · 2018-12-20
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器械摘要
常见问题
What is the FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute?
FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute is a medical device that received FDA 510(k) clearance on 2018-12-20. The listed applicant is Prosidyan, Inc.. The 510(k) number is K182670.
When did FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute receive FDA 510(k) clearance?
FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute received FDA 510(k) clearance on 2018-12-20, under 510(k) number K182670.
Who is the listed applicant for FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute?
The FDA 510(k) record lists Prosidyan, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute?
The FDA product code for FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute is MQV.
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。
列明Prosidyan, Inc.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:MQV)
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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