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INTESS LUMBAR CAGE

Page Type
Cleared 510(K)
510(k) Number
K123100
510(k) Type
Traditional
Applicant
KALITEC DIRECT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2013
Days to Decision
177 days
Submission Type
Summary

INTESS LUMBAR CAGE

Page Type
Cleared 510(K)
510(k) Number
K123100
510(k) Type
Traditional
Applicant
KALITEC DIRECT, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2013
Days to Decision
177 days
Submission Type
Summary