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INTEGRA LAMINOPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130830
510(k) Type
Traditional
Applicant
SEASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2013
Days to Decision
44 days
Submission Type
Summary

INTEGRA LAMINOPLASTY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K130830
510(k) Type
Traditional
Applicant
SEASPINE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2013
Days to Decision
44 days
Submission Type
Summary