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Genesys Spine 3DP Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K182987
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2019
Days to Decision
409 days
Submission Type
Summary

Genesys Spine 3DP Lumbar Interbody System

Page Type
Cleared 510(K)
510(k) Number
K182987
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/2019
Days to Decision
409 days
Submission Type
Summary