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

REFORM PEDICLE SCREW SYSTEM

K Number: K131343 · Decision Jul 24, 2013
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
23
Review Days
76

Basic Information

Device Name
REFORM PEDICLE SCREW SYSTEM
K Number
K131343
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SPINAL USA
Date Received
May 9, 2013
Decision Date
July 24, 2013
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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