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Orthotech
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Known Names
orthotech co, orthotech
Recent 510(k) Clearances
K-Number
Device
Date
K971453
ORTHOTEC K-CAP SYSTEM
June 24, 1997
K933080
ORTHOTECH DURA-GOLD BARCKETS
March 23, 1994