FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LAMOREUX-OSI ELECTROGONIOMETER

K Number: K831040 · Decision Jul 12, 1983
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
32
Applicant Total
95
Review Days
103

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Basic Information

Device Name
LAMOREUX-OSI ELECTROGONIOMETER
K Number
K831040
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.1500
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Orthopedic Systems, Inc.
Date Received
March 31, 1983
Decision Date
July 12, 1983
Product Code
KQX
Advisory Committee
Orthopedic
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
KQX Goniometer, Ac-Powered

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K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K892503 NUFFIELD TOTAL KNEE
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
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