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Half Dome Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K152512
510(k) Type
Traditional
Applicant
Astura Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
148 days
Submission Type
Summary

Half Dome Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K152512
510(k) Type
Traditional
Applicant
Astura Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
148 days
Submission Type
Summary