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

Sniper Spine System

K Number: K152174 · Decision Aug 31, 2015
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
40
Review Days
27

Basic Information

Device Name
Sniper Spine System
K Number
K152174
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SPINE WAVE, INC.
Date Received
August 4, 2015
Decision Date
August 31, 2015
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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K Number Device Name
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K152620 Spine Wave Gen II Expandable Interbody System
K151813 Sniper Spine System
K151581 Leva Spacer System
K150285 Leva(TM) Spacer System
K142996 StaXx(R) XD System
K141980 LEVA (TM) SPACER SYSTEM
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