34 results
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53ms
·
Sources: EU EUDAMED, US FDA
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
Medtronic (Changzhou) Medical Devices Technology Co., Ltd·3 products·🇨🇳 China
DIVERGENCE-L Anterior/Oblique Lumbar Fusion System
FDA registration
Sterigenics US, LLC·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·3 products·🇩🇪 Germany
STERIS ISOMEDIX PUERTO RICO, INC.
FDA registration
STERIS ISOMEDIX PUERTO RICO, INC.·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
WARSAW ORTHOPEDIC, INC.·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·3 products·🇺🇸 United States
intervertebral fusion device with bone graft, lumbar
FDA registration
MedTorque, Inc·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·3 products·🇺🇸 United States
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·3 products·🇮🇳 India
Synergy Health Allershausen GmbH
FDA registration
Synergy Health Allershausen GmbH·3 products·🇩🇪 Germany
DIVERGENCE-L" ANTERIOR/OBLIQUE LUMBAR FUSION SYSTEM
FDA registration
Medtronic Medical Costa Rica S.R.L.·3 products·🇨🇷 Costa Rica
DIVERGENCE-L Anterior/Oblique Lumbar Fusion System
FDA 510(k)
FDA Class 2
·Orthopedic
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169502413·SCREW 2150135 SCREW 35MM
RUSCH
FDA UDI
TELEFLEX INCORPORATED·14026704711823·Rusch Polaris FO Blade, Mac 3.5
RUSCH
FDA UDI
TELEFLEX INCORPORATED·14026704629708·Rusch Polaris FO Blade, Mac 3.5
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117506·Distal Reamer (Hudson)
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690111627·Modular Stem 13mm x 150mm
TiLock
FDA UDI
Genesys Orthopedics Systems LLC·M719G1501350·Pre-Bent Rod
Guide Catheter 14FR GDS Accucinch System
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States