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OAKTREE Anterior Lumbar Plate and Screw System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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