Zenith Dissection Endovascular System
FDA premarket approval P180001/S004 · decided 2022-04-14
Approval details
- PMA number
- P180001
- Supplement
- S004
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Zenith Dissection Endovascular System
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- William Cook Europe Aps
- Date received
- 2022-03-18
- Decision date
- 2022-04-14
- Days to decision
- 27 days
- Decision code
- APPR
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bjaeverskov
- Statement
- Approval for an additional seal on one side of the Zenith Dissection Endovascular Graft primary packaging and new specifications for the position of an already applied seal on the opposite side.
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.