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ASTRA Spine System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211323
510(k) Type
Special
Applicant
Spinecraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2021
Days to Decision
34 days
Submission Type
Summary

ASTRA Spine System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211323
510(k) Type
Special
Applicant
Spinecraft, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2021
Days to Decision
34 days
Submission Type
Summary