Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K971996
Device Classification Name
Arthroscope
More FDA Info for this Device
510(K) Number
K971996
Device Name
Arthroscope
Applicant
MEDIVISION SCOPE SERVICE CENTER, INC.
1440 S. STATE COLLEGE BLVD.
#1D
ANAHEIM, CA 92806 US
Other 510(k) Applications for this Company
Contact
WAYNE B STERNER
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
05/30/1997
Decision Date
07/31/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact