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DRPx Locking Distal Radius Plate System

Page Type
Cleared 510(K)
510(k) Number
K212601
510(k) Type
Traditional
Applicant
Orthopaedic Implant Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2022
Days to Decision
231 days
Submission Type
Summary

DRPx Locking Distal Radius Plate System

Page Type
Cleared 510(K)
510(k) Number
K212601
510(k) Type
Traditional
Applicant
Orthopaedic Implant Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2022
Days to Decision
231 days
Submission Type
Summary