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

DURACON PS LIPPED TIBIAL INSERT

K Number: K012172 · Decision Oct 10, 2001
Classifications
1
FEI Numbers
320
Registration Numbers
320
Same Product Code
902
Applicant Total
13
Review Days
90

Basic Information

Device Name
DURACON PS LIPPED TIBIAL INSERT
K Number
K012172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
HOWMEDICA OSTEONICS
Date Received
July 12, 2001
Decision Date
October 10, 2001
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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Other Clearances by HOWMEDICA OSTEONICS

K Number Device Name
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K033258 BONESAVE BONE VOID FILLER
K032855 STRYKER SPINE MAPS SYSTEM
K031702 REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K031435 BONESOURCE BVF
K031217 GMRS PRESS FIT STEMS WITH PUREFIX HA
K022461 S2 FEMORAL NAIL
K022160 XIA SPINAL SYSTEM
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