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

TIMESH SELF DRILLING SCREW

K Number: K062348 · Decision Sep 8, 2006
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
28
Review Days
28

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Basic Information

Device Name
TIMESH SELF DRILLING SCREW
K Number
K062348
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Neurosurgery
Date Received
August 11, 2006
Decision Date
September 8, 2006
Product Code
HWC
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
HWC Screw, Fixation, Bone

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