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

FOUNDATION MODULAR TIBIAL BASEPLATE

K Number: K932425 · Decision Jul 22, 1994
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
85
Review Days
429

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Basic Information

Device Name
FOUNDATION MODULAR TIBIAL BASEPLATE
K Number
K932425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Encore Orthopedics, Inc.
Date Received
May 19, 1993
Decision Date
July 22, 1994
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 Encore Orthopedics, Inc.

K Number Device Name
K032905 3DKNEE POROUS COATED FEMORAL COMPONENT
K020114 3D KNEE
K020741 UNICONDYLAR KNEE
K020236 MODIFICATION TO PASS SPINAL SYSTEM
K020170 KEYSTONE HIP SYSTEM CALCAR REPLACEMENT BODY AND BUILD UP
K013490 CEMENTED CALCAR HIP SYSTEM
K013442 PASS SPINAL SYSTEM
K003324 PLASMA SPRAYED SHOULDER
K013431 PASS SPINAL SYSTEM
K013191 PASS SPINAL SYSTEM
Search all 85 clearances from Encore Orthopedics, Inc. →