FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP

K Number: K925181 · Decision Feb 5, 1993
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
44
Applicant Total
31
Review Days
114

Basic Information

Device Name
TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
K Number
K925181
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3320
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
TECHMEDICA, INC.
Date Received
October 14, 1992
Decision Date
February 5, 1993
Product Code
JDL
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
JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

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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
K920080 CONTINUUM KNEE SYSTEM
K921458 TMP MICROPLATING SYSTEM
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