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

IMPROVED PASSIVATION METHOD FOR METALLIC ORTHOPAEDIC IMPLANTS

K Number: K934590 · Decision Jun 14, 1995
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
87
Review Days
628

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Basic Information

Device Name
IMPROVED PASSIVATION METHOD FOR METALLIC ORTHOPAEDIC IMPLANTS
K Number
K934590
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew Richards, Inc.
Date Received
September 24, 1993
Decision Date
June 14, 1995
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other Clearances by Smith & Nephew Richards, Inc.

K Number Device Name
K965224 EMPOWER ANTERIOR DIRECT SCREWS
K963509 GLOBAL TAPER TAPERED HIP SYSTEM, GT SPECTRON
K960444 FINN ROD TO ROD CONNECTOR
K964163 TRIMAX NAIL SYSTEM
K962557 GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENT
K963486 REVISION HIP SYSTEM
K962541 REFLECTION ACETABULAR REINFORCEMENT RINGS
K962808 ILIZAROV EXTERNAL FIXATION SYSTEM
K962137 GENESIS II CONSTRAINED SYSTEM
K955767 COFIED MODULAR SHOULDER SYSTEM
Search all 87 clearances from Smith & Nephew Richards, Inc. →