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

TIBIA-TALUS-CALCANEUS NAIL

K Number: K950394 · Decision May 19, 1995
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
87
Review Days
107

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TIBIA-TALUS-CALCANEUS NAIL
K Number
K950394
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew Richards, Inc.
Date Received
February 1, 1995
Decision Date
May 19, 1995
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

Similar 510(k) Clearances

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

View all

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. →