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ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223301
510(k) Type
Traditional
Applicant
SpineCraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
266 days
Submission Type
Summary

ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223301
510(k) Type
Traditional
Applicant
SpineCraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2023
Days to Decision
266 days
Submission Type
Summary