FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE

K Number: K051827 · Decision Aug 12, 2005
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
7
Review Days
37

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Basic Information

Device Name
JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE
K Number
K051827
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Joimax GmbH
Date Received
July 6, 2005
Decision Date
August 12, 2005
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HRX Arthroscope

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