Zenith® Dissection Endovascular System
FDA premarket approval P180001/S003 · decided 2021-12-15
Approval details
- PMA number
- P180001
- Supplement
- S003
- Supplement type
- 30-Day Notice
- 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
- 2021-11-15
- Decision date
- 2021-12-15
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Bjaeverskov
- Statement
- Change to the delivery system trigger-wire coating facility and updates to the acceptance criteria used in testing of the trigger wires.
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