K-number	K081673
Device name	DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE
Applicant	Ionics Medical Corp.
Product code	MAX
Device class	Class II
Decision date	Nov 14, 2008
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE

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