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

CONCEPT UNICOMPARTMENTAL KNEE SYSTEM

K Number: K896648 · Decision Jun 5, 1990
Classifications
1
FEI Numbers
156
Registration Numbers
156
Same Product Code
109
Applicant Total
83
Review Days
193

Basic Information

Device Name
CONCEPT UNICOMPARTMENTAL KNEE SYSTEM
K Number
K896648
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
CONCEPT, INC.
Date Received
November 24, 1989
Decision Date
June 5, 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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K891109 PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE
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