Epic Extremity, LLC is one of 18463 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epic Extremity, LLC - FDA 510(k) Cleared Devices
Recent clearances: EPIC Extremity Fusion Plate System, EPIC Extremity Fracture Plate System, EPIC Extremity Snap-Off Screw
5
Total
5
Cleared
0
Denied
Epic Extremity, LLC has 5 FDA 510(k) cleared medical devices. Based in Cranberry Twp, US.
Historical record: 5 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Epic Extremity, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intrepid Orthopedics, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Epic Extremity, LLC
5 devices
Cleared
Feb 13, 2019
EPIC Extremity Fusion Plate System
Orthopedic
107d
Cleared
Nov 06, 2017
EPIC Extremity Fracture Plate System
Orthopedic
87d
Cleared
Feb 28, 2017
EPIC Extremity Snap-Off Screw
Orthopedic
120d
Cleared
Feb 09, 2016
Epic Extremity Plate System
Orthopedic
82d
Cleared
Jan 19, 2016
Epic Extremity Cannulated Screw System
Orthopedic
61d