FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SPECIALIST(R) WALKER

K Number: K924984 · Decision Feb 1, 1993
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
7
Applicant Total
22
Review Days
123

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Basic Information

Device Name
SPECIALIST(R) WALKER
K Number
K924984
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.3910
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Johnson & Johnson Orthopaedics, Inc.
Date Received
October 1, 1992
Decision Date
February 1, 1993
Product Code
FYH
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FYH Splint, Extremity, Noninflatable, External, Sterile

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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
K931054 TRICK MODULAR KNEE TIBIAL TRAY-POROUS
Search all 22 clearances from Johnson & Johnson Orthopaedics, Inc. →