Last synced on 14 November 2025 at 11:06 pm

FUSELOX LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K122956
510(k) Type
Special
Applicant
CAPTIVA SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2012
Days to Decision
30 days
Submission Type
Summary

FUSELOX LUMBAR INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K122956
510(k) Type
Special
Applicant
CAPTIVA SPINE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2012
Days to Decision
30 days
Submission Type
Summary