Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)— 510(k) K173352
Substantially EquivalentConcentric Medical, Inc.
FDA 510(k) clearance K173352 for Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever), Substantially Equivalent on 2018-02-15. Applicant: Concentric Medical, Inc..
Clearance details
- Applicant
- Concentric Medical, Inc.
- Product code
- Code POL
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mountain View, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.