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

VERTEBRON PSS PEDICLE SCREW SYSTEM

K Number: K043152 · Decision Feb 1, 2005
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
11
Review Days
78

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Basic Information

Device Name
VERTEBRON PSS PEDICLE SCREW SYSTEM
K Number
K043152
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
November 15, 2004
Decision Date
February 1, 2005
Product Code
MNH
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
MNH Orthosis, Spondylolisthesis Spinal Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNH), 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
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
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. →