Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME AND XIENCE PRIME LL EVEROLIMUS ELUTING CORNARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM AND XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE Alpine Everolimus Eluting Coronary Stent System, XIENCE Sierra Everolimus Eluting Coronary Stent System, XIENCE S

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME & XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEMS

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM,XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE Xpedition, XIENCE Xpedition SV, XIENCE Xpedition LL Everolimus Eluting Coronary Stent Systems

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·Xience Skypoint Everolimus Eluting Coronary Stent System; XIENCE Alpine Everolimus Coronary Stent System; XIENCE Sierra

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM, XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME AND XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE Sierra Stent System

Coronary Drug-Eluting Stent

FDA Pre-Market Approval

FDA Class 3 ·XIENCE PRIME EECSS (XIENCE PRIME AND XIENCE PRIME LONG LENGTHS [LL])

Electrode, Needle

FDA classification

FDA Class 2 ·Electrode, Needle

Coronary Drug-Eluting Stent

FDA classification

FDA Class 3 ·Coronary Drug-Eluting Stent

Laser, Ophthalmic

FDA classification

FDA Class 2 ·Laser, Ophthalmic

Patella Trial <41> mm SFP (264-1-10041)

FDA registration

Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration

STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia