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Arthronics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K931107
LOGYK ACETABULAR COMPONENT SYSTEM
March 28, 1994
K921382
FUTURA TEXTURE-TRAKKED TOTAL HIP STEM
January 7, 1994