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Axiom Worldwide, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K060735DRX9000 TRUE SPINAL DECOMPRESSION SYSTEMMay 26, 2006
K051135AXIOM NVP8500August 11, 2005
K050687AXIOM EPS8000July 28, 2005
K010292DRX 2000May 1, 2001