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ASTRA Spine System

Page Type
Cleared 510(K)
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)
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