FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

System, Endovascular Graft, Aortic Aneurysm Treatment

PMA: P070007 · Decision Jun 5, 2008
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
System, Endovascular Graft, Aortic Aneurysm Treatment
Trade Name
TALENT THORACIC STENT GRAFT SYSTEM
PMA Number
P070007
Device Class
FDA Class 3
Product Code
MIH
Generic Name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved (Withdrawn)
Decision Code
APWD
Decision Date
June 5, 2008
Date Received
March 1, 2007
Expedited Review
N
Docket Number
08M-0342

Advisory Committee Statement

APPROVAL FOR THE TALENT THORACIC STENT GRAFT SYSTEM. THE DEVICE IS INDICATED FOR THE ENDOVASCULAR REPAIR OF FUSIFORM ANEURYSMS AND SACCULAR ANEURYSMS/ PENETRATING ULCERS OF THE DESCENDING THORACIC AORTA IN PATIENTS HAVING APPROPRIATE ANATOMY, INCLUDING: 1) ILIAC/FEMORAL ACCESS VESSEL MORPHOLOGY THAT IS COMPATIBLE WITH VASCULAR ACCESS TECHNIQUES, DEVICES, AND/OR ACCESSORIES; 2) NON-ANEURYSMAL AORTIC DIAMETER IN THE RANGE OF 18-42MM; AND 3) NON-ANEURYSMAL AORTIC PROXIMAL AND DISTAL NECK LENGTHS >=20MM.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MIH System, Endovascular Graft, Aortic Aneurysm Treatment