Last synced on 14 November 2025 at 11:06 pm

SPINAL USA INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K080314
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
97 days
Submission Type
Summary

SPINAL USA INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K080314
510(k) Type
Traditional
Applicant
SPINAL USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2008
Days to Decision
97 days
Submission Type
Summary