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Genesys Spine 3DP Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191489
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2020
Days to Decision
218 days
Submission Type
Summary

Genesys Spine 3DP Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191489
510(k) Type
Traditional
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2020
Days to Decision
218 days
Submission Type
Summary