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

GSB ELBOW

K Number: K901581 · Decision Oct 22, 1990
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
28
Applicant Total
16
Review Days
201

Basic Information

Device Name
GSB ELBOW
K Number
K901581
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3150
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
ALLO PRO CORP.
Date Received
April 4, 1990
Decision Date
October 22, 1990
Product Code
JDC
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
JDC Prosthesis, Elbow, Constrained, Cemented

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