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Genesys Spine 3DP Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K220096
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2022
Days to Decision
56 days
Submission Type
Summary

Genesys Spine 3DP Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K220096
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/2022
Days to Decision
56 days
Submission Type
Summary