Fx Solutions is one of 285 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Fx Solutions - FDA 510(k) Cleared Devices
Recent clearances: Humeris Shoulder, Humelock Reversed Shoulder, Humelock II Reversible Shoulder System
8
Total
8
Cleared
0
Denied
Fx Solutions has 8 FDA 510(k) cleared medical devices. Based in Viriat, FR.
Historical record: 8 cleared submissions from 2011 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Fx Solutions Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ferguson Medical International Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Fx Solutions
8 devices
Cleared
May 17, 2017
Humeris Shoulder
Orthopedic
141d
Cleared
Jan 17, 2017
Humelock Reversed Shoulder
Orthopedic
137d
Cleared
Nov 13, 2015
Humelock II Reversible Shoulder System
Orthopedic
261d
Cleared
Aug 27, 2015
PRCT2
Orthopedic
241d
Cleared
Jul 28, 2014
HUMELOCK II CEMENTED SHOULDER SYSTEM
Orthopedic
196d
Cleared
Nov 09, 2013
HUMELOCK II CEMENTLESS SHOULDER SYSTEM
Orthopedic
234d
Cleared
Aug 13, 2013
HUMELOCK II CEMENTED SHOULDER SYSTEM
Orthopedic
244d
Cleared
Nov 09, 2011
HUMELOCK CEMENTED SHOULDER PROSTHESIS
Orthopedic
203d