Last synced on 14 November 2025 at 11:06 pm

HALF DOME Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K163481
510(k) Type
Traditional
Applicant
Astura Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
142 days
Submission Type
Summary

HALF DOME Posterior Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K163481
510(k) Type
Traditional
Applicant
Astura Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2017
Days to Decision
142 days
Submission Type
Summary