Cleared Traditional

K051676 - SPINEASSIST DEVICE WITH ADDITIONAL ACCESSORIES

K051676 is an FDA 510(k) clearance for SPINEASSIST DEVICE WITH ADDITIONAL ACCE..., manufactured by Mazor Surgical Technologies , Ltd.. The device is a Class 2 Neurology device with product code HAW cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K051676 · Mazor Surgical Technologies , Ltd. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2005
Decision
77d
Days
Class 2
Risk

K051676 is an FDA 510(k) clearance for the SPINEASSIST DEVICE WITH ADDITIONAL ACCESSORIES. Classified as Neurological Stereotaxic Instrument (product code HAW), Class II - Special Controls.

Submitted by Mazor Surgical Technologies , Ltd. (Kfar Saba, IL). The FDA issued a Cleared decision on September 8, 2005 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.4560 - the FDA neurology device 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 Mazor Surgical Technologies , Ltd. devices

FDA 510(k) Submission Details - K051676

510(k) Number K051676 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2005
Decision Date September 08, 2005
Days to Decision 77 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
71d faster than avg
Panel avg: 148d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HAW Device Classification - Class 2, Special Controls

Product Code HAW Neurological Stereotaxic Instrument
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.4560
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 Neurology devices follow this clearance model.

Regulatory Peers - HAW Neurological Stereotaxic Instrument

All 278
Devices cleared under the same product code (HAW) and FDA review panel - the closest regulatory comparables to K051676.
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MEDTRONIC ORTHOPAEDIC TRAUMA APPLICATION
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ELEKTA ESARTE FRAME SYSTEM
K051746 · Elekta Instrument AB · Jul 2005
ACUMEN IMAGE GUIDED SURGICAL SYSTEM
K051724 · Ebi, L.P. · Jul 2005