5,634 results
·
25ms
·
Sources: EU EUDAMED, US FDA
K2M, Inc.
Manufacturer
🇺🇸 United States·1 Importer
K2M, INC.
FDA registration
K2M, INC.·46 products·🇺🇸 United States
dental diamond bur
FDA UDI
STRAUSS & CO - INDUSTRIAL DIAMONDS LTD·D877K2M6·Dental Diamond Bur
GM-K2 M
Device
EU MDR
·
Eu Md Class 1
·PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság·On the market
K2M COCR ROD
FDA 510(k)
FDA Class 2
·Orthopedic
K2M MODULAR HOOKS
FDA 510(k)
FDA Class 2
·Orthopedic
K2M Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
K2M Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
K2M COCR WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
K2M Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
K2M Expandable Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
K2M Growing Spine System
FDA 510(k)
FDA Class 2
·Orthopedic
K2M Fenestrated Tap System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
K2M Patient Specific Rods
FDA 510(k)
FDA Class 2
·Orthopedic
Brainlab Compatible K2M Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
K2M, PYRENEES CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Brainlab Compatible K2M Navigation Instruments
FDA 510(k)
FDA Class 2
·Neurology
K2M GEARSHIFT
FDA Adverse Event
Malfunction
·K2M, INC.·Product code MAX·May 30, 2018
EVEREST ® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·STRYKER-SPINE·Product code LXH·September 9, 2019
K2M NAVIGATION INSTRUMENTS
FDA Adverse Event
Malfunction
·K2M, INC.·Product code OLO·November 16, 2017