Last synced on 25 April 2025 at 11:05 pm

ROVO Mechanical Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220780
510(k) Type
Traditional
Applicant
2MG, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
379 days
Submission Type
Summary

ROVO Mechanical Thrombectomy Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220780
510(k) Type
Traditional
Applicant
2MG, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2023
Days to Decision
379 days
Submission Type
Summary