Last synced on 14 November 2025 at 11:06 pm

PRADO™ Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K252113
510(k) Type
Special
Applicant
Bethesda Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2025
Days to Decision
29 days
Submission Type
Summary

PRADO™ Lumbar Interbody Fusion System

Page Type
Cleared 510(K)
510(k) Number
K252113
510(k) Type
Special
Applicant
Bethesda Medical Devices
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2025
Days to Decision
29 days
Submission Type
Summary