FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

RANGE SPINAL SYSTEM

K Number: K130330 · Decision May 2, 2013
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
18
Applicant Total
100
Review Days
80

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Basic Information

Device Name
RANGE SPINAL SYSTEM
K Number
K130330
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
K2m, Inc.
Date Received
February 11, 2013
Decision Date
May 2, 2013
Product Code
OSH
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
OSH Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis

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