K-number	K182210
Device name	TiWAVE-L Porous Titanium Lumbar Cage
Applicant	Kalitec Medical, LLC
Product code	MAX
Device class	Class II
Decision date	Jan 7, 2019
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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TiWAVE-L Porous Titanium Lumbar Cage

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