K-number	K112556
Device name	ADM AND ADM/MDM DURATION INSERTS, ADM AND ADM/MDM X3 INSERTS
Applicant	Howmedica Osteonics Corp.
Product code	MEH
Device class	Class II
Decision date	Sep 28, 2011
Decision	Substantially Equivalent
Regulation	888.3353

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View the full FDA submission: accessdata.fda.gov

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ADM AND ADM/MDM DURATION INSERTS, ADM AND ADM/MDM X3 INSERTS

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