Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever
K-Number: K203219 · 2020-12-29
Device Summary
Frequently Asked Questions
What is the Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever?
Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever is a medical device that received FDA 510(k) clearance on 2020-12-29. It is manufactured by Stryker Neurovascular. The 510(k) number is K203219.
When was Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever approved by the FDA?
Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever received FDA 510(k) clearance on 2020-12-29, under approval number K203219.
What company makes Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever?
Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever is manufactured by Stryker Neurovascular.
What is the FDA product code for Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever?
The FDA product code for Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever is POL.
Related Clinical Trials
Other Devices by Stryker Neurovascular
Related Devices (Code: POL)
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.