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

CUP, ACETABULAR, LONG POSTERIOR WALL

K Number: K780398 · Decision Mar 21, 1978
Classifications
1
FEI Numbers
231
Registration Numbers
231
Same Product Code
560
Applicant Total
45
Review Days
8

Basic Information

Device Name
CUP, ACETABULAR, LONG POSTERIOR WALL
K Number
K780398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
ORTHOPEDIC EQUIPMENT CO., INC.
Date Received
March 13, 1978
Decision Date
March 21, 1978
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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