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

VUSION CS PLUS

K Number: K122588 · Decision Jun 12, 2013
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
45
Review Days
292

Basic Information

Device Name
VUSION CS PLUS
K Number
K122588
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Development Corp.
Date Received
August 24, 2012
Decision Date
June 12, 2013
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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