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ATEC Posterior Navigated Disc Prep Instruments

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