Last synced on 25 April 2025 at 11:05 pm

SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153783
510(k) Type
Traditional
Applicant
SpineVision S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/4/2016
Days to Decision
125 days
Submission Type
Summary

SpaceVision® PLIF, SpaceVision® OLIF, SpaceVision® TLIF

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K153783
510(k) Type
Traditional
Applicant
SpineVision S.A.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
5/4/2016
Days to Decision
125 days
Submission Type
Summary