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

ORTHOPAEDIC CABLE SYSTEM

K Number: K842977 · Decision Oct 26, 1984
Classifications
1
FEI Numbers
153
Registration Numbers
153
Same Product Code
127
Applicant Total
71
Review Days
88

Basic Information

Device Name
ORTHOPAEDIC CABLE SYSTEM
K Number
K842977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
RICHARDS MEDICAL CO., INC.
Date Received
July 30, 1984
Decision Date
October 26, 1984
Product Code
JDQ
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
JDQ Cerclage, Fixation

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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.
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