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

FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE

K Number: K051000 · Decision May 19, 2005
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
33
Review Days
29

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Basic Information

Device Name
FORTITUDE VUE VERTEBRAL BODY REPLACEMENT DEVICE
K Number
K051000
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spinal Concepts, Inc.
Date Received
April 20, 2005
Decision Date
May 19, 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 Spinal Concepts, Inc.

K Number Device Name
K050706 HARMONY PORT SYSTEM, MODEL 1907 SERIES
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K033663 SPINAL CONCEPTS INC. CODA
K033517 SPINAL CONCEPTS INC. CADENCE AND TRAXIS
K031855 SPINAL CONCEPTS, INC. INSIGHT PEDICLE SCREW SYSTEM
K031985 SPINAL CONCEPTS INC. NEX-LINK SPINAL FIXATION SYSTEM
K031318 TRAXIS CEMENT RESTRICTOR
K031672 SPINAL CONCEPTS, INC. INFIX SYSTEM
K031837 MODIFICATION TO FORTITUDE CEMENT RESTRICTOR
K030087 SPINAL CONCEPTS, INC. BACFIX TI SPINAL SYSTEM
Search all 33 clearances from Spinal Concepts, Inc. →