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ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM

Spineart · Class II · Cleared Aug 19, 2011

K-numberK112108
Device nameROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
ApplicantSpineart
Product codeMNI
Device classClass II
Decision dateAug 19, 2011
DecisionSubstantially Equivalent
Regulation888.3070
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View the full FDA submission: accessdata.fda.gov

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