FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

SODEM HIGH SPEED SYSTEM (ELECTRIC) (GENERAL ORTHOPEDICS & PLASTIC SURGERY)

K Number: K012453 · Decision Oct 22, 2001
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
25
Applicant Total
6
Review Days
82

Basic Information

Device Name
SODEM HIGH SPEED SYSTEM (ELECTRIC) (GENERAL ORTHOPEDICS & PLASTIC SURGERY)
K Number
K012453
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4360
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SODEM SYSTEMS
Date Received
August 1, 2001
Decision Date
October 22, 2001
Product Code
HBC
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
HBC Motor, Drill, Electric

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Other Clearances by SODEM SYSTEMS

K Number Device Name
K023070 SODEM HIGH SPEED SYSTEM (PNEUMATIC)
K023066 DRILL GUIDE ATTACHMENT (PN 3105 DG) OF THE SODEM HIGH SPEED SYSTEM (PNEUMATIC)
K012457 SODEM HIGH SPEED SYSTEM (ELECTRIC) (NEURO/SPINE SURGERY)
K012456 SODEM HIGH SPEED SYSTEM (ELECTRIC) (EAR, NOSE, AND THROAT)
K994175 MODIFICATION TO SODEM HIGH SPEED SYSTEM FOR NEUROSURGICAL USE