Last synced on 14 November 2025 at 11:06 pm

CancelleX Porous Titanium Lumbar Interbody Device

Page Type
Cleared 510(K)
510(k) Number
K190364
510(k) Type
Traditional
Applicant
Xenco Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2019
Days to Decision
62 days
Submission Type
Summary

CancelleX Porous Titanium Lumbar Interbody Device

Page Type
Cleared 510(K)
510(k) Number
K190364
510(k) Type
Traditional
Applicant
Xenco Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2019
Days to Decision
62 days
Submission Type
Summary