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

RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS

K Number: K893377 · Decision Nov 16, 1989
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
71
Review Days
199

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Basic Information

Device Name
RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS
K Number
K893377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Richards Medical Co., Inc.
Date Received
May 1, 1989
Decision Date
November 16, 1989
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

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Other Clearances by Richards Medical Co., Inc.

K Number Device Name
K896106 ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTS
K900628 MODULAR HIP SYSTEM
K896580 UNI-POLAR HEAD
K895241 INTRAMEDULLARY HIP SCREW
K884824 TRICON-M TOTAL KNEE SYSTEM
K896204 ZIRCONIA CERAMIC HEAD ADD'L SIZES
K895242 PAPPAS TRI-FLANGE VENTILATION TUBE
K885069 ZIRCONIA CERAMIC HEAD (YITRIA STABILIZED)
K892366 POROUS GENESIS STEMMED TIBIAL COMPONENT
K890132 POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP.
Search all 71 clearances from Richards Medical Co., Inc. →