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INTESS CERVICAL CAGE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133815
510(k) Type
Traditional
Applicant
KALITEC DIRECT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2014
Days to Decision
121 days
Submission Type
Summary

INTESS CERVICAL CAGE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K133815
510(k) Type
Traditional
Applicant
KALITEC DIRECT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2014
Days to Decision
121 days
Submission Type
Summary