Kentrospine Viktr-MIS® Pedicle screw system
K号: K252139 · 2026-09-27
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器械摘要
Kentrospine Viktr-MIS® Pedicle screw system is the device name listed in this FDA 510(k) record. The listed applicant is Rivarp Medical Pvt., Ltd.. It received FDA 510(k) clearance on 2026-09-27 under 510(k) number K252139. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Kentrospine Viktr-MIS® Pedicle screw system?
Kentrospine Viktr-MIS® Pedicle screw system is a medical device that received FDA 510(k) clearance on 2026-09-27. The listed applicant is Rivarp Medical Pvt., Ltd.. The 510(k) number is K252139.
When did Kentrospine Viktr-MIS® Pedicle screw system receive FDA 510(k) clearance?
Kentrospine Viktr-MIS® Pedicle screw system received FDA 510(k) clearance on 2026-09-27, under 510(k) number K252139.
Who is the listed applicant for Kentrospine Viktr-MIS® Pedicle screw system?
The FDA 510(k) record lists Rivarp Medical Pvt., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kentrospine Viktr-MIS® Pedicle screw system?
The FDA product code for Kentrospine Viktr-MIS® Pedicle screw system is NKB.
相关临床试验
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相关器械（代码：NKB）
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。
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官方来源
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