Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments
K号: K230873 · 2023-08-01
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器械摘要
常见问题
What is the Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments?
Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments is a medical device that received FDA 510(k) clearance on 2023-08-01. The listed applicant is Southern Implants (Pty), Ltd.. The 510(k) number is K230873.
When did Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments receive FDA 510(k) clearance?
Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments received FDA 510(k) clearance on 2023-08-01, under 510(k) number K230873.
Who is the listed applicant for Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments?
The FDA 510(k) record lists Southern Implants (Pty), Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments?
The FDA product code for Angulated Screw Channel (ASC) Solution Abutments & SI-BASE Abutments is NHA.
相关临床试验
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列明Southern Implants (Pty), 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:NHA)
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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