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FDA 510(k) Application Details - K953978
Device Classification Name
Appliance, Fixation, Spinal Intervertebral Body
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510(K) Number
K953978
Device Name
Appliance, Fixation, Spinal Intervertebral Body
Applicant
ACROMED CORP.
3303 CARNEGIE AVE.
CLEVELAND, OH 44115 US
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Contact
GREGORY CANNEDY
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Regulation Number
888.3060
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Classification Product Code
KWQ
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More FDA Info for this Product Code
Date Received
08/23/1995
Decision Date
02/19/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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