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FDA 510(k) Application Details - K990324
Device Classification Name
Arthroscope
More FDA Info for this Device
510(K) Number
K990324
Device Name
Arthroscope
Applicant
NUVASIVE, INC.
13221 MARICOTTE PLACE
SAN DIEGO, CA 92130 US
Other 510(k) Applications for this Company
Contact
STEVE REITZLER
Other 510(k) Applications for this Contact
Regulation Number
888.1100
More FDA Info for this Regulation Number
Classification Product Code
HRX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/02/1999
Decision Date
10/05/1999
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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