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FDA 510(k) Application Details - K954411
Device Classification Name
Stimulator, Muscle, Powered
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510(K) Number
K954411
Device Name
Stimulator, Muscle, Powered
Applicant
ZIMMER ELEKTROMEDIZIN GMBH
9 JUNKERSSTRABE
D7910 NEU-ULM DE
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Contact
DUCHESS GRANGER
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Regulation Number
890.5850
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Classification Product Code
IPF
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More FDA Info for this Product Code
Date Received
09/21/1995
Decision Date
02/28/1996
Decision
SN - Substantially Equivalent for Some Indications
Classification Advisory Committee
PM - Physical Medicine
Review Advisory Committee
PM - Physical Medicine
Statement / Summary / Purged Status
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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