Cleared Traditional

K933244 - DISPOSABLE GRASPING FORCEP

K933244 is an FDA 510(k) clearance for DISPOSABLE GRASPING FORCEP, manufactured by Neuro Navigational Corp.. The device is a Class 2 Neurology device with product code GWG cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K933244 · Neuro Navigational Corp. · Neurology device
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Sep 1993
Decision
70d
Days
Class 2
Risk

K933244 is an FDA 510(k) clearance for the DISPOSABLE GRASPING FORCEP. Classified as Endoscope, Neurological (product code GWG), Class II - Special Controls.

Submitted by Neuro Navigational Corp. (Costa Mesa, US). The FDA issued a Cleared decision on September 10, 1993 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.1480 - 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 Neuro Navigational Corp. devices

FDA 510(k) Submission Details - K933244

510(k) Number K933244 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 1993
Decision Date September 10, 1993
Days to Decision 70 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 148d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GWG Device Classification - Class 2, Special Controls

Product Code GWG Endoscope, Neurological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.1480
Definition If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 - GWG Endoscope, Neurological

All 67
Devices cleared under the same product code (GWG) and FDA review panel - the closest regulatory comparables to K933244.
CODMAN QUICK SHUNT KIT, CAT. #82-6570
K934196 · Codman & Shurtleff, Inc. · Apr 1994
CODMAN LASER NEUROENDOSCOPE
K924977 · Codman & Shurtleff, Inc. · Nov 1993
DISPOSABLE PEEL-AWAY INTRODUCER SHEATH
K931973 · Neuro Navigational Corp. · Sep 1993
CODMAN ENDOFLEX GRASPING AND BIOPSY FORCEPS
K923646 · Codman & Shurtleff, Inc. · Dec 1992