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

MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM

K Number: K081597 · Decision Jul 2, 2008
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
11
Review Days
26

Basic Information

Device Name
MODIFICATION TO VERTEBRON PSS PEDICLE SCREW SYSTEM
K Number
K081597
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VERTEBRON, INC.
Date Received
June 6, 2008
Decision Date
July 2, 2008
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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K Number Device Name
K081567 VERTEBRON SSP CERVICAL PLATING SYSTEM
K073502 VERTEBRON VBR 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. →