Last synced on 14 November 2025 at 11:06 pm

EMBOTRAP III Revascularization Device

Page Type
Cleared 510(K)
510(k) Number
K251789
510(k) Type
Special
Applicant
Neuravi Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
9/25/2025
Days to Decision
106 days
Submission Type
Summary

EMBOTRAP III Revascularization Device

Page Type
Cleared 510(K)
510(k) Number
K251789
510(k) Type
Special
Applicant
Neuravi Limited
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
9/25/2025
Days to Decision
106 days
Submission Type
Summary