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INTERMEDICS ORTHOPEDICS SAW BLADE

Intermedics Orthopedics · Class I · Cleared Nov 18, 1993

K-numberK931210
Device nameINTERMEDICS ORTHOPEDICS SAW BLADE
ApplicantIntermedics Orthopedics
Product codeGFA
Device classClass I
Decision dateNov 18, 1993
DecisionSubstantially Equivalent
Regulation878.4820
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View the full FDA submission: accessdata.fda.gov

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