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

MANTIS REDUX SPINAL SYSTEM

K Number: K092631 · Decision Sep 25, 2009
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
64
Review Days
30

Basic Information

Device Name
MANTIS REDUX SPINAL SYSTEM
K Number
K092631
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STRYKER SPINE
Date Received
August 26, 2009
Decision Date
September 25, 2009
Product Code
NKB
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
NKB Thoracolumbosacral Pedicle Screw System

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