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

NOVEL VBR SPINAL SYSTEM

K Number: K042201 · Decision Oct 7, 2004
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
9
Review Days
55

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Basic Information

Device Name
NOVEL VBR SPINAL SYSTEM
K Number
K042201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec/Nexmed
Date Received
August 13, 2004
Decision Date
October 7, 2004
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 Alphatec/Nexmed

K Number Device Name
K050830 ZODIAC SPINAL FIXATION SYSTEM
K051286 ZODIAC SPINAL FIXATION SYSTEM
K050553 NOVEL VBR SPINAL SYSTEM
K050390 TAMARACK ANTERIOR THORACOLUNBAR
K050078 ROC LUMBAR PLATING SYSTEM
K042252 NEXFLEX TOTAL HIP SYSTEM
K042673 ZODIAC POLYAXIAL SPINAL FIXATION SYSTEM
K042440 ALPHATEC FEMORAL TROCHANTERIC NAIL (FTN) SYSTEM