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

VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS

K Number: K062666 · Decision Jan 25, 2007
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
45
Review Days
140

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Basic Information

Device Name
VUSION TS, PS, AND CS PARTIAL VERTEBRAL BODY REPLACEMENTS
K Number
K062666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ortho Development Corp.
Date Received
September 7, 2006
Decision Date
January 25, 2007
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

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