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FDA 510(k) Application Details - K994363
Device Classification Name
Arthroscope
More FDA Info for this Device
510(K) Number
K994363
Device Name
Arthroscope
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
353 CORPORATE WOODS PKWY.
VERNON HILLS, IL 60061 US
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Contact
ROBERT L CASARSA
Other 510(k) Applications for this Contact
Regulation Number
888.1100
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Classification Product Code
HRX
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More FDA Info for this Product Code
Date Received
12/27/1999
Decision Date
03/06/2000
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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