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

ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)

K Number: K083161 · Decision Mar 27, 2009
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
21
Review Days
151

Basic Information

Device Name
ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)
K Number
K083161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
CONMED LINVATEC
Date Received
October 27, 2008
Decision Date
March 27, 2009
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

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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