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

CONCORDE VBR SPINAL SYSTEM

K Number: K052746 · Decision Oct 21, 2005
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
68
Review Days
21

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Basic Information

Device Name
CONCORDE VBR SPINAL SYSTEM
K Number
K052746
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Depuy Spine, Inc.
Date Received
September 30, 2005
Decision Date
October 21, 2005
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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Other Clearances by Depuy Spine, Inc.

K Number Device Name
K201831 CONFIDENCE Spinal Cement System
K142185 EXPEDIUM VERSE SPINE SYSTEM
K111136 EXPEDIUM SPINE SYSTEM, VIPER SYSTEM, VIPER 2 SYSTEM
K121020 VIPER SYSTEM
K110353 MOUNTAINEER OCT SPINAL SYSTEM
K110216 EXPEDIUM SYSTEM, VIPER SYSTEM
K103133 VEPER SYSTEM, EXPEDIUM SYSTEM
K101993 VIPER SYSTEM, EXPEDIUM SYSTEM
K103100 MOUNTAINEER OCT SPINAL SYSTEM
K101762 VIPER F2 FACET FIXATION SYSTEM
Search all 68 clearances from Depuy Spine, Inc. →