Accelerated Innovation, LLC

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K081127ACCIN TOTAL KNEE SYSTEMOctober 17, 2008
K080647ACCIN BIPOLAR HEAD SYSTEMJuly 8, 2008
K080539ACCIN UNIPOLAR HEAD SYSTEMJune 2, 2008
K073120ACCIN PATELLOFEMORAL SYSTEMFebruary 29, 2008
K073531ACCIN PEDICLE SCREW SYSTEMFebruary 4, 2008
K073530ACCIN ANTERIOR CERVICAL PLATE SYSTEMJanuary 31, 2008
K073068ACCIN HIP SYSTEMJanuary 10, 2008