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

TRICK MODULAR KNEE TIBIAL TRAY-POROUS

K Number: K931054 · Decision Jan 25, 1994
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
22
Review Days
330

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Basic Information

Device Name
TRICK MODULAR KNEE TIBIAL TRAY-POROUS
K Number
K931054
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Johnson & Johnson Orthopaedics, Inc.
Date Received
March 1, 1993
Decision Date
January 25, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JWH), ordered by most recent decision date.

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Other Clearances by Johnson & Johnson Orthopaedics, Inc.

K Number Device Name
K931466 PFC MODULAR TOTAL KNEE SYSTEM, POROUS COATED SACRI
K935452 P.F.C. 2 TOTAL HIP SYSTEM POROUS COATED MODULAR FEMORAL COMPONENT
K940190 ULTIMA UNIPOLAR MODULAR HEAD
K933275 P.F.C. CERAMIC HIP HEAD
K932595 ORTHOSORB(TM) ABSORBABLE CEMENT RESTRICTOR
K931655 P.F.C. BIPOLAR HIP SYSTEM
K933867 UNIVERSAL INSET PATELLA
K935262 P.F.C. TOTAL KNEE SYSTEM OVAL PATELLA
K931189 P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET
K924340 P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT
Search all 22 clearances from Johnson & Johnson Orthopaedics, Inc. →