OVATION AND OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
FDA premarket approval P120006/S009 · decided 2014-04-23
Approval details
- PMA number
- P120006
- Supplement
- S009
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- OVATION AND OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- Endologix, LLC
- Date received
- 2013-11-12
- Decision date
- 2014-04-23
- Days to decision
- 162 days
- Decision code
- APPR
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Rosa, CA
- Statement
- APPROVAL FOR A CHANGE TO THE INDICATION FOR USE FOR THE OVATION AND OVATION PRIME ABDOMINAL STENT GRAFT SYSTEMS BY CLARIFYING THAT PERCUTANEOUS ACCESS AND FEMORAL CUTDOWN ARE APPROPRIATE VASCULAR ACCESS TECHNIQUES. THE DEVICE, THE TRIVASCULAR OVATION AND OVATION PRIME ABDOMINAL STENT GRAFT SYSTEM, IS INDICATED FOR TREATMENT OF PATIENTS WITH ABDOMINAL AORTIC ANEURYSMS HAVING THE VASCULAR MORPHOLOGY SUITABLE FOR ENDOVASCULAR REPAIR, INCLUDING:1) ADEQUATE ILIAC/FEMORAL ACCESS COMPATIBLE WITH VASCUL
Class III intelligence, same tools
PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.