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FDA 510(k)

Solitare Platinum Revascularization Device

K-Number: K181186 · 2018-10-25

ApplicantMicro Therapeutics, Inc. d/b/a ev3 Neurovascular
Decision Date2018-10-25
Product CodePOL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Solitare Platinum Revascularization Device is a medical device manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. It received FDA 510(k) clearance on 2018-10-25 under approval number K181186. The device is classified under product code POL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Solitare Platinum Revascularization Device?

Solitare Platinum Revascularization Device is a medical device that received FDA 510(k) clearance on 2018-10-25. It is manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular. The 510(k) number is K181186.

When was Solitare Platinum Revascularization Device approved by the FDA?

Solitare Platinum Revascularization Device received FDA 510(k) clearance on 2018-10-25, under approval number K181186.

What company makes Solitare Platinum Revascularization Device?

Solitare Platinum Revascularization Device is manufactured by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular.

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

The FDA product code for Solitare Platinum Revascularization Device is POL.

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Other Devices by Micro Therapeutics, Inc. d/b/a ev3 Neurovascular

K162539Solitaire 2 Revascularization Device K161152Navien Intracranial Support Catheter K161879Solitaire Platinum Revascularization Device K172448Riptide Aspiration System K171268Reverse 021 Micro Catheter, Reverse 027 Micro Catheter K160641Solitaire Platinum Revascularization Device, 6x40 mm

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Related Devices (Code: POL)

K162539Solitaire 2 Revascularization DeviceMicro Therapeutics, Inc. d/b/a ev3 Neurovascular DEN150049Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP ProVue Retriever 3x20mm, Trevo XP ProVue Retriever 6x25mm, Trevo XP ProVue Retriever 4x30mmConcentric Medical, Inc. K181060Solitaire 2 and Solitaire Platinum Revascularization DeviceMedtronic Neurovascular K173352Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)Concentric Medical, Inc. K192207Trevo NXT ProVue RetrieverStryker K190779Trevo XP ProVue RetrieverStryker

Official Source

View on FDA Database →

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

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