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

MCCUTCHEN ACETABULAR CUP PROSTHESIS

K Number: K872732 · Decision Oct 1, 1987
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
560
Applicant Total
74
Review Days
85

Basic Information

Device Name
MCCUTCHEN ACETABULAR CUP PROSTHESIS
K Number
K872732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
DOW CORNING WRIGHT
Date Received
July 8, 1987
Decision Date
October 1, 1987
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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