Last synced on 16 May 2025 at 11:05 pm

Genesys Spine 3DP AIS-C II Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233594
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
35 days
Submission Type
Summary

Genesys Spine 3DP AIS-C II Cervical Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233594
510(k) Type
Special
Applicant
Genesys Spine
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
35 days
Submission Type
Summary