Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever— 510(k) K203219
Substantially EquivalentStryker Neurovascular
FDA 510(k) clearance K203219 for Trevo XP ProVue Retriever and Trevo NXT ProVue Retriever, Substantially Equivalent on 2020-12-29. Applicant: Stryker Neurovascular. Device class: 2.
Clearance details
- Applicant
- Stryker Neurovascular
- Product code
- Code POL
- Device class
- Class 2
- Regulation
- 21 CFR 882.5600
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Fremont, CA, US
Recent devices under product code POL
view allMore clearances from Stryker Neurovascular
view all- K261889 — Trevo Trak 21 Microcatheter
- K253032 — AXS Lift Intracranial Base Catheter
- K252694 — Target Detachable Coil
- K251832 — InZone IST Detachment System; IZDS Connecting Cable
- K242289 — Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27 Pre-Shaped Microcatheter, Excelsior XT-27 Flex Pre-Shaped Microcatheter
Data sourced from openFDA. This site is unofficial and independent of the FDA.