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ATEC Posterior Navigated Disc Prep Instruments

Page Type
Cleared 510(K)
510(k) Number
K232345
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
90 days
Submission Type
Summary

ATEC Posterior Navigated Disc Prep Instruments

Page Type
Cleared 510(K)
510(k) Number
K232345
510(k) Type
Traditional
Applicant
Alphatec Spine, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
90 days
Submission Type
Summary