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ASTRA-OCT Spine System

Page Type
Cleared 510(K)
510(k) Number
K181350
510(k) Type
Traditional
Applicant
SpineCraft LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2018
Days to Decision
45 days
Submission Type
Summary

ASTRA-OCT Spine System

Page Type
Cleared 510(K)
510(k) Number
K181350
510(k) Type
Traditional
Applicant
SpineCraft LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2018
Days to Decision
45 days
Submission Type
Summary