Medical Device Manufacturer · US , Leesburg , VA

K2m, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005
8
Total
8
Cleared
0
Denied

K2m, LLC has 8 FDA 510(k) cleared medical devices. Based in Leesburg, US.

Historical record: 8 cleared submissions from 2005 to 2018. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by K2m, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by K2m, LLC

8 devices
1-8 of 8
Cleared Nov 28, 2018
SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System
K180665 · MQP
Orthopedic · 259d
Cleared May 22, 2014
EVEREST SPINAL SYSTEM
K140529 · NKB
Orthopedic · 79d
Cleared May 23, 2006
DENALI DEFORMITY SYSTEM
K052404 · KWP
Orthopedic · 264d
Cleared May 15, 2006
PYRENEES CERVICAL PLATE SYSTEM
K060442 · KWQ
Orthopedic · 83d
Cleared Dec 07, 2005
MESA SPINAL SYSTEM
K052398 · MNI
Orthopedic · 98d
Cleared Oct 17, 2005
TECTONIC CERVICAL PLATE SYSTEM
K051531 · KWQ
Orthopedic · 130d
Cleared Jul 27, 2005
ALEUTIAN SPACER SYSTEM
K051454 · MQP
Orthopedic · 55d
Cleared Jan 10, 2005
DENALI SPINE SYSTEM
K042635 · KWP
Orthopedic · 105d
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