Trevo NXT ProVue Retriever— 510(k) K223305
Substantially EquivalentStryker Neurovascular
FDA 510(k) clearance K223305 for Trevo NXT ProVue Retriever, Substantially Equivalent on 2023-03-29. Applicant: Stryker Neurovascular. Device class: 2.
Clearance details
- Applicant
- Stryker Neurovascular
- Product code
- Product 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
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view allRecalls naming K223305
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K223305.
Data sourced from openFDA. This site is unofficial and independent of the FDA.