Sonoma Orthopedic Products, Inc. is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonoma Orthopedic Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Sonoma Fifth Metatarsal Repair System, Sonoma Fibula Repair System, SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC XXYYY(X=DIA, YYY=LENGTH- IN MM)
9
Total
9
Cleared
0
Denied
Sonoma Orthopedic Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Santa Rosa, US.
Historical record: 9 cleared submissions from 2008 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sonoma Orthopedic Products, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mrc-X, LLC and Memphis Regulatory Consulting, LLC.
FDA 510(k) Regulatory Record - Sonoma Orthopedic Products, Inc.
9 devices
Cleared
Feb 24, 2017
Sonoma Fifth Metatarsal Repair System
Orthopedic
283d
Cleared
Jan 22, 2015
Sonoma Fibula Repair System
Orthopedic
104d
Cleared
Aug 19, 2011
SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC...
Orthopedic
77d
Cleared
Sep 28, 2010
SOMONA CWG CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA CWG XYYY(X=DIA,...
Orthopedic
257d
Cleared
Jan 20, 2010
WAVEON FRACTURE REPAIR SYSTEM (WAVEON RX)
Orthopedic
190d
Cleared
Aug 28, 2009
WAVEON WRX BONE FIXATION SYSTEM
Orthopedic
203d
Cleared
Oct 10, 2008
ENSPLINTCMX CLAVICLE PIN
Orthopedic
105d
Cleared
Jul 10, 2008
ENSPLINT TM BONE SCREW
Orthopedic
113d
Cleared
Feb 21, 2008
ENSPLINTRX BONE FIXATION SYSTEM
Orthopedic
234d