Last synced on 14 November 2025 at 11:06 pm

LDR SPINE ROI INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082262
510(k) Type
Traditional
Applicant
LDR SPINE USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2009
Days to Decision
178 days
Submission Type
Summary

LDR SPINE ROI INTERBODY FUSION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082262
510(k) Type
Traditional
Applicant
LDR SPINE USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2009
Days to Decision
178 days
Submission Type
Summary