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

AIS Odontoid Fracture Fixation System

K Number: K142707 · Decision Dec 19, 2014
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
18
Review Days
88

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Basic Information

Device Name
AIS Odontoid Fracture Fixation System
K Number
K142707
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aesculap Implant System, Inc.
Date Received
September 22, 2014
Decision Date
December 19, 2014
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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K130291 S4 SPINAL SYSTEM
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K112551 S4 SPINAL SYSTEM
K101281 VEGA KNEE SYSTEM
K100147 S4 CERVICAL OCCIPITAL PLATE SPINAL SYSTEM
Search all 18 clearances from Aesculap Implant System, Inc. →