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Solar Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231199
510(k) Type
Traditional
Applicant
DeGen Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
50 days
Submission Type
Summary

Solar Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K231199
510(k) Type
Traditional
Applicant
DeGen Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/2023
Days to Decision
50 days
Submission Type
Summary