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

CRYSTAL

K Number: K073351 · Decision Jan 24, 2008
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
49
Review Days
56

Basic Information

Device Name
CRYSTAL
K Number
K073351
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
November 29, 2007
Decision Date
January 24, 2008
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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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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