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

VERTEBRON VBR SYSTEM

K Number: K073502 · Decision Mar 24, 2008
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
11
Review Days
102

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Basic Information

Device Name
VERTEBRON VBR SYSTEM
K Number
K073502
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vertebron, Inc.
Date Received
December 13, 2007
Decision Date
March 24, 2008
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQP), ordered by most recent decision date.

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Other Clearances by Vertebron, Inc.

K Number Device Name
K081567 VERTEBRON SSP CERVICAL PLATING SYSTEM
K081597 MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
K071376 MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
K062110 VERTEBRON SCP CERVICAL PLATE SYSTEM
K051815 MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
K051716 VERTEBRON PSS PEDICLE SCREW SYSTEM
K043152 VERTEBRON PSS PEDICLE SCREW SYSTEM
K043181 MODIFICATION TO VERTEBRON SCP CERVICAL PLATE SYSTEM
K040003 VERTEBRON SCP CERVICAL PLATE SYSTEM
K033352 VERTEBRON PSS PEDICLE SCREW SYSTEM
Search all 11 clearances from Vertebron, Inc. →