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FDA 510(k)

MS Lide Implant Systems

K-Number: K181477 · 2020-10-20

ApplicantHangzhou Minsheng Lide Medical Science & Technology Co., Ltd.
Decision Date2020-10-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MS Lide Implant Systems is a medical device manufactured by Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-10-20 under approval number K181477. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS Lide Implant Systems?

MS Lide Implant Systems is a medical device that received FDA 510(k) clearance on 2020-10-20. It is manufactured by Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd.. The 510(k) number is K181477.

When was MS Lide Implant Systems approved by the FDA?

MS Lide Implant Systems received FDA 510(k) clearance on 2020-10-20, under approval number K181477.

What company makes MS Lide Implant Systems?

MS Lide Implant Systems is manufactured by Hangzhou Minsheng Lide Medical Science & Technology Co., Ltd..

What is the FDA product code for MS Lide Implant Systems?

The FDA product code for MS Lide Implant Systems is DZE.

Related Clinical Trials

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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