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

COROENT SMALL INTERBODY SYSTEM

K Number: K140003 · Decision Apr 3, 2014
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
91
Review Days
91

Basic Information

Device Name
COROENT SMALL INTERBODY SYSTEM
K Number
K140003
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
January 2, 2014
Decision Date
April 3, 2014
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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