Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Micro Therapeutics Lnc. D/B/A Ev3 Neurovascular · Predicate Candidate Screening

3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K241177React 71 CatheterMicro Therapeutics Lnc. D/B/A Ev3 Neurovascular2024-05-28290
K233420Axium Detachable Coil; Axium Prime Detachable CoilMicro Therapeutics Lnc. D/B/A Ev3 Neurovascular2023-11-07280
K210230Phenom CathetersMicro Therapeutics Lnc. D/B/A Ev3 Neurovascular2021-02-25280

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda