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INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133418
510(k) Type
Traditional
Applicant
SEASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2014
Days to Decision
175 days
Submission Type
Summary

INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133418
510(k) Type
Traditional
Applicant
SEASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2014
Days to Decision
175 days
Submission Type
Summary