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SIRION Lateral Lumbar Interbody Fusion

Page Type
Cleared 510(K)
510(k) Number
K202495
510(k) Type
Traditional
Applicant
Astura Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2021
Days to Decision
128 days
Submission Type
Summary

SIRION Lateral Lumbar Interbody Fusion

Page Type
Cleared 510(K)
510(k) Number
K202495
510(k) Type
Traditional
Applicant
Astura Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/2021
Days to Decision
128 days
Submission Type
Summary