Last synced on 25 April 2025 at 11:05 pm

Sacrix® Sacroiliac Joint Fusion Device System, Inspan® ScrewLES Fusion System, Invue® MAX™ + Invue Inset Anterior Cervical Plate System, and FacetFuse® Screw Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232605
510(k) Type
Special
Applicant
LESspine Innovations
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2023
Days to Decision
31 days
Submission Type
Summary

Sacrix® Sacroiliac Joint Fusion Device System, Inspan® ScrewLES Fusion System, Invue® MAX™ + Invue Inset Anterior Cervical Plate System, and FacetFuse® Screw Fixation System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232605
510(k) Type
Special
Applicant
LESspine Innovations
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2023
Days to Decision
31 days
Submission Type
Summary