K2m - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
K2m has 16 FDA 510(k) cleared orthopedic devices. Based in Leesburg, US.
Historical record: 16 cleared submissions from 2014 to 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by K2m
16 devices
Cleared
Nov 15, 2018
YUKON OCT Spinal System
Orthopedic
94d
Cleared
Nov 09, 2018
Brainlab Compatible K2M Navigation Instruments
Orthopedic
119d
Cleared
Feb 12, 2018
CASCADIA Interbody System
Orthopedic
139d
Cleared
Jan 16, 2018
K2M Navigation Instruments
Orthopedic
231d
Cleared
Jan 09, 2018
Everest Spinal System
Orthopedic
57d
Cleared
Aug 31, 2017
CAPRI Corpectomy Cage System
Orthopedic
84d
Cleared
Aug 30, 2017
K2M Navigation Instruments
Orthopedic
118d
Cleared
Apr 13, 2017
CAPRI Corpectomy Cage System
Orthopedic
97d
Cleared
Mar 15, 2017
MOJAVE Expandable Interbody System
Orthopedic
105d
Cleared
Apr 27, 2016
Pyrenees Cervical Plate System
Orthopedic
140d
Cleared
Apr 22, 2016
Cascadia Interbody System
Orthopedic
93d
Cleared
Mar 24, 2016
Cascadia Interbody System
Orthopedic
27d
Cleared
Jan 05, 2016
K2M Fenestrated Tap System
Gastroenterology & Urology
97d
Cleared
Sep 24, 2015
Pyrenees Cervical Plate System
Orthopedic
43d
Cleared
Jul 14, 2015
Pyrenees Cervical Plate System
Orthopedic
91d
Cleared
Dec 22, 2014
Caspian OCT/MESA Mini/DENALI Mini Spinal System
Orthopedic
102d