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TiWAVE-L Porous Titanium Lumbar Cage

Page Type
Cleared 510(K)
510(k) Number
K182210
510(k) Type
Traditional
Applicant
Kalitec Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2019
Days to Decision
145 days
Submission Type
Summary

TiWAVE-L Porous Titanium Lumbar Cage

Page Type
Cleared 510(K)
510(k) Number
K182210
510(k) Type
Traditional
Applicant
Kalitec Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2019
Days to Decision
145 days
Submission Type
Summary