Cleared Traditional

K160003 - Sniper (R) Spine System

K160003 is an FDA 510(k) clearance for Sniper Spine System, manufactured by Spine Wave, Inc.. The device is a Class 2 Orthopedic device with product code MNI cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K160003 · Spine Wave, Inc. · Orthopedic device
Download Printable Device Report (PDF)
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Feb 2016
Decision
53d
Days
Class 2
Risk

K160003 is an FDA 510(k) clearance for the Sniper (R) Spine System. Classified as Orthosis, Spinal Pedicle Fixation (product code MNI), Class II - Special Controls.

Submitted by Spine Wave, Inc. (Shelton, US). The FDA issued a Cleared decision on February 26, 2016 after a review of 53 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3070 - the FDA orthopedic device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Spine Wave, Inc. devices

FDA 510(k) Submission Details - K160003

510(k) Number K160003 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 04, 2016
Decision Date February 26, 2016
Days to Decision 53 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 122d · This submission: 53d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MNI Device Classification - Class 2, Special Controls

Product Code MNI Orthosis, Spinal Pedicle Fixation
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3070
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - MNI Orthosis, Spinal Pedicle Fixation

All 260
Devices cleared under the same product code (MNI) and FDA review panel - the closest regulatory comparables to K160003.
MySpine Pedicle Screw Placement Guides - LP
K153273 · Medacta International S.A. · Jun 2016
LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation System
K160124 · Spinevision S.A. · Apr 2016
Premier
K160320 · Shandong Weigao Orthopaedic Device Co., Ltd. · Apr 2016
YAHUA Spinal System
K152324 · Beijing Weigao Yahua Artificial Joint Development Co. , Ltd. · Feb 2016
FIREFLY Pedicle Screw Navigation Guide
K143222 · Mighty Oak Medical, Inc. · Dec 2015
WASTON General Spinal System
K150684 · Changzhou Waston Medical Appliance Co., Ltd. · Nov 2015