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

CONTINUUM KNEE SYSTEM (CKS)-MODIFICATION

K Number: K903286 · Decision Oct 12, 1990
Classifications
1
FEI Numbers
156
Registration Numbers
156
Same Product Code
109
Applicant Total
31
Review Days
88

Basic Information

Device Name
CONTINUUM KNEE SYSTEM (CKS)-MODIFICATION
K Number
K903286
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
TECHMEDICA, INC.
Date Received
July 16, 1990
Decision Date
October 12, 1990
Product Code
HSX
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
HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

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Other Clearances by TECHMEDICA, INC.

K Number Device Name
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K931929 TECHMEDICA CONTINUUM HIP SYSTEM
K926387 TECHMEDICA STANDARD CEMENTED HIP SYSTEM
K925420 TECHMEDICA STANDARD BIPOLAR SYSTEM
K923808 MULLER STRAIGHT STEM FEMORAL PROSTHESIS
K926579 TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE
K911058 TECHMEDICA CAD/CAM CUSTOM HIP
K925181 TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
K920080 CONTINUUM KNEE SYSTEM
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