Last synced on 25 April 2025 at 11:05 pm

Genesys Spine 3DP Lumbar Interbody System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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