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ATEC Lateral Plate System

Page Type
Cleared 510(K)
510(k) Number
K230721
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2023
Days to Decision
55 days
Submission Type
Summary

ATEC Lateral Plate System

Page Type
Cleared 510(K)
510(k) Number
K230721
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2023
Days to Decision
55 days
Submission Type
Summary