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HALF DOME Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K182877
510(k) Type
Traditional
Applicant
Astura Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
200 days
Submission Type
Summary

HALF DOME Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K182877
510(k) Type
Traditional
Applicant
Astura Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2019
Days to Decision
200 days
Submission Type
Summary