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

KINEMATIC III POST CRUCIATE TOTAL CONDYLAR KNEE SY

K Number: K871772 · Decision Jun 3, 1987
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
373
Review Days
28

Basic Information

Device Name
KINEMATIC III POST CRUCIATE TOTAL CONDYLAR KNEE SY
K Number
K871772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
HOWMEDICA CORP.
Date Received
May 6, 1987
Decision Date
June 3, 1987
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

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K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
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K983419 HOFFMANN II MIAMI POST
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