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

VERTE-STACK SPINAL SYSTEM

K Number: K070173 · Decision Mar 14, 2007
Classifications
1
FEI Numbers
215
Registration Numbers
215
Same Product Code
275
Applicant Total
96
Review Days
55

Basic Information

Device Name
VERTE-STACK SPINAL SYSTEM
K Number
K070173
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDTRONIC SOFAMOR DANEK, INC.
Date Received
January 18, 2007
Decision Date
March 14, 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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