VLP Wrist Fracture System
K号: K161665 · 2016-11-15
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器械摘要
VLP Wrist Fracture System is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2016-11-15 under 510(k) number K161665. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VLP Wrist Fracture System?
VLP Wrist Fracture System is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K161665.
When did VLP Wrist Fracture System receive FDA 510(k) clearance?
VLP Wrist Fracture System received FDA 510(k) clearance on 2016-11-15, under 510(k) number K161665.
Who is the listed applicant for VLP Wrist Fracture System?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VLP Wrist Fracture System?
The FDA product code for VLP Wrist Fracture System is HRS.
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列明Smith & Nephew, 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。
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相关器械（代码：HRS）
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官方来源
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