Last synced on 14 November 2025 at 11:06 pm

EPICAGE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130548
510(k) Type
Special
Applicant
ALPHATEC SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2013
Days to Decision
45 days
Submission Type
Summary

EPICAGE INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K130548
510(k) Type
Special
Applicant
ALPHATEC SPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2013
Days to Decision
45 days
Submission Type
Summary