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

RICHARDS EXTERNAL FIXATION SYSTEM

K Number: K870961 · Decision Mar 19, 1987
Classifications
1
FEI Numbers
247
Registration Numbers
247
Same Product Code
392
Applicant Total
71
Review Days
9

Basic Information

Device Name
RICHARDS EXTERNAL FIXATION SYSTEM
K Number
K870961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
RICHARDS MEDICAL CO., INC.
Date Received
March 10, 1987
Decision Date
March 19, 1987
Product Code
KTT
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
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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K Number Device Name
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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
K893377 RUSSELL-TAYLOR INTRAMEDULLARY KNEE FUSION NAILS
K885069 ZIRCONIA CERAMIC HEAD (YITRIA STABILIZED)
K890132 POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP.
Search all 71 clearances from RICHARDS MEDICAL CO., INC. →