Orthopro, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122936ANKLE TRAUMA SYSTEMFebruary 28, 2013
K113006I-FUSE HAMMER TOE SYSTEMSMay 25, 2012
K093055CSTS SCREWNovember 22, 2010
K073228DC ULNAR SHORTENING SYSTEMFebruary 29, 2008
K070555ORTHOPRO STEINMAN PINS AND KIRSCHNER WIRESJuly 13, 2007
K071243METAL HEMI IMPLANTMay 23, 2007
K062908ORTHROPRO HEMI TOENovember 13, 2006