FDA 510(k)

Solitaire Platinum Revascularization Device

K号: K161879 · 2016-09-21

申请人Micro Therapeutics, Inc. d/b/a ev3 Neurovascular

决定日期2016-09-21

产品代码NRY

咨询委员会CV

决定Substantially Equivalent

器械摘要

Solitaire Platinum Revascularization Device is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. It received FDA 510(k) clearance on 2016-09-21 under 510(k) number K161879. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Solitaire Platinum Revascularization Device?

Solitaire Platinum Revascularization Device is a medical device that received FDA 510(k) clearance on 2016-09-21. The listed applicant is Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. The 510(k) number is K161879.

When did Solitaire Platinum Revascularization Device receive FDA 510(k) clearance?

Solitaire Platinum Revascularization Device received FDA 510(k) clearance on 2016-09-21, under 510(k) number K161879.

Who is the listed applicant for Solitaire Platinum Revascularization Device?

The FDA 510(k) record lists Micro Therapeutics, Inc. d/b/a ev3 Neurovascular as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Solitaire Platinum Revascularization Device?

The FDA product code for Solitaire Platinum Revascularization Device is NRY.

列明Micro Therapeutics, Inc. d/b/a ev3 Neurovascular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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