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

SPINAL ELEMENTS CERCLAGE SYSTEM

K Number: K120177 · Decision Jul 3, 2012
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
49
Review Days
165

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Basic Information

Device Name
SPINAL ELEMENTS CERCLAGE SYSTEM
K Number
K120177
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Elements, Inc.
Date Received
January 20, 2012
Decision Date
July 3, 2012
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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Other Clearances by Spinal Elements, Inc.

K Number Device Name
K260506 Ventana® P/T Lumbar Interbody System
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K250773 Luna® Ti Interbody Fusion System
K242527 The Karma® Fixation System
K243916 Primus Spinal Fixation System
K231593 Sapphire X3 Anterior Cervical Plate System
K231252 Ventana™ L Spinal System
K222833 Ventana™ C Spinal System
K222516 Mercury® II Spinal System
K210044 Crystal Spinal System & Vertu Spinal System, Lucent Spinal System, Zeus Spinal System, Ceres-C Spinal System, Omega XP Spinal System
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