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ExtremiLOCK Lateral Ankle Fusion Plates

Page Type
Cleared 510(K)
510(k) Number
K203479
510(k) Type
Traditional
Applicant
OsteoMed
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
89 days
Submission Type
Summary

ExtremiLOCK Lateral Ankle Fusion Plates

Page Type
Cleared 510(K)
510(k) Number
K203479
510(k) Type
Traditional
Applicant
OsteoMed
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2021
Days to Decision
89 days
Submission Type
Summary