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DRPx Locking Distal Radius Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202971
510(k) Type
Traditional
Applicant
Orthopaedic Implant Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2021
Days to Decision
218 days
Submission Type
Summary

DRPx Locking Distal Radius Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202971
510(k) Type
Traditional
Applicant
Orthopaedic Implant Company
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/6/2021
Days to Decision
218 days
Submission Type
Summary