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

QUANTUM/STREAMLINE TL MIS SPINAL SYSTEM

K Number: K093771 · Decision Aug 10, 2010
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
50
Review Days
245

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Basic Information

Device Name
QUANTUM/STREAMLINE TL MIS SPINAL SYSTEM
K Number
K093771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pioneer Surgical Technology
Date Received
December 8, 2009
Decision Date
August 10, 2010
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

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