COMPANY
Contego Medical
Timeline
- FDA FDA 510(k) clearance: Excipio LV Prime Thrombectomy Device — K251485, Jun 13, 2025. Applicant at approval: Contego Medical, Inc. source ↗
- FDA FDA PMA approval: Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection — P240009, Oct 11, 2024. Applicant at approval: Contego Medical, Inc. source ↗
FDA records (last 2 years)
- FDA 510(k) clearance: Excipio LV Prime Thrombectomy Device — K251485, Jun 13, 2025. Applicant at approval: Contego Medical, Inc. source ↗
- FDA PMA approval: Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection — P240009, Oct 11, 2024. Applicant at approval: Contego Medical, Inc. source ↗
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