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Headless Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K200259
510(k) Type
Special
Applicant
OsteoCentric Extremities, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2020
Days to Decision
91 days
Submission Type
Summary

Headless Compression Screw System

Page Type
Cleared 510(K)
510(k) Number
K200259
510(k) Type
Special
Applicant
OsteoCentric Extremities, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/4/2020
Days to Decision
91 days
Submission Type
Summary