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Hand Innovations, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061748FRAGMENT PLATE SYSTEMJuly 17, 2006
K060864MULTIDIRECTIONAL THREADED PEGApril 28, 2006
K060294DIAPHYSEAL PLATEMarch 22, 2006
K060290SHOULDER FIXATION SYSTEMFebruary 27, 2006
K052294SHOULDER NAIL PLATEOctober 21, 2005
K052248DORSAL NAIL PLATE, ANATOMICALSeptember 14, 2005
K051728MODIFICATION TO SHOULDER FIXATION SYSTEMJuly 20, 2005
K050932DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEMApril 26, 2005
K042059SHOULDER FIXATION SYSTEMSeptember 30, 2004
K041157MODIFICATION TO SMALL BONE FIXATION SYSTEMJuly 30, 2004
K041081FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRESJuly 1, 2004
K033406SMALL BONE FIXATION SYSTEMJanuary 15, 2004
K032705DISTAL RADIUS FRACTURE REPAIR SYSTEMOctober 1, 2003
K030198HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEMApril 1, 2003
K023007DISTAL RADIUS FRACTURE REPAIR SYSTEMDecember 5, 2002
K013424INTRAMEDULLARY FIXATION SYSTEM FOR THE HANDDecember 20, 2001
K002775DISTAL VOLAR RADIUS FRACTURE REPAIR SYSTEMDecember 5, 2000