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

MOSAIC DEVICES

K Number: K071833 · Decision Oct 23, 2007
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
49
Review Days
112

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Basic Information

Device Name
MOSAIC DEVICES
K Number
K071833
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Elements, Inc.
Date Received
July 3, 2007
Decision Date
October 23, 2007
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

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Other Clearances by Spinal Elements, Inc.

K Number Device Name
K260506 Ventana® P/T Lumbar Interbody System
K253559 Ventana™ A Anterior Lumbar Interbody System
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
Search all 49 clearances from Spinal Elements, Inc. →