Zenith Dissection Endovascular System
FDA premarket approval P180001/S002 · decided 2021-03-31
Approval details
- PMA number
- P180001
- Supplement
- S002
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Labeling Change - PAS
- Trade name
- Zenith Dissection Endovascular System
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- William Cook Europe Aps
- Date received
- 2020-10-02
- Decision date
- 2021-03-31
- Days to decision
- 180 days
- Decision code
- APPR
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bjaeverskov
- Statement
- Approval of the labeling updates for the post-approval study (PAS) protocol.
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