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

NUFFIELD TOTAL KNEE

K Number: K892503 · Decision May 4, 1990
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
95
Review Days
388

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Basic Information

Device Name
NUFFIELD TOTAL KNEE
K Number
K892503
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Orthopedic Systems, Inc.
Date Received
April 11, 1989
Decision Date
May 4, 1990
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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Other Clearances by Orthopedic Systems, Inc.

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K910736 JACKSON MULTIPURPOSE OPERATING TABLE
K910031 PARK CITY SHOULDER POSITIONER
K903938 C FIT CUP
K896678 SILICONE PLUG
K894283 COMPREHENSIVE SPINE MOTION ANALYZER
K890498 FREEMAN MODULAR HIP STEM RIDGED VERSION
K890331 FREEMAN TOTAL HIP SYSTEM RIDGED STEM
K895217 CORTICAL SCREW
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