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OAKTREE Anterior Lumbar Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K220843
510(k) Type
Traditional
Applicant
Oak Tree Engineering, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2022
Days to Decision
259 days
Submission Type
Summary

OAKTREE Anterior Lumbar Plate and Screw System

Page Type
Cleared 510(K)
510(k) Number
K220843
510(k) Type
Traditional
Applicant
Oak Tree Engineering, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2022
Days to Decision
259 days
Submission Type
Summary