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CODA™ Anterior Cervical Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230993
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2023
Days to Decision
75 days
Submission Type
Summary

CODA™ Anterior Cervical Plate System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230993
510(k) Type
Special
Applicant
Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2023
Days to Decision
75 days
Submission Type
Summary