Cleared Traditional

K963893 - FIBRE INTERSPACED X-RAY GRID

K963893 is an FDA 510(k) clearance for FIBRE INTERSPACED X-RAY GRID, manufactured by Smit Rontgen. The device is a Class 1 Radiology device with product code IXJ cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K963893 · Smit Rontgen · Radiology device
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Nov 1996
Decision
41d
Days
Class 1
Risk

K963893 is an FDA 510(k) clearance for the FIBRE INTERSPACED X-RAY GRID. Classified as Grid, Radiographic (product code IXJ), Class I - General Controls.

Submitted by Smit Rontgen (Md Eindhoven, NL). The FDA issued a Cleared decision on November 7, 1996 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1910 - the FDA radiology and imaging software oversight 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 Smit Rontgen devices

FDA 510(k) Submission Details - K963893

510(k) Number K963893 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 27, 1996
Decision Date November 07, 1996
Days to Decision 41 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 107d · This submission: 41d
Pathway characteristics
Predicate-based equivalence.

IXJ Device Classification - Class 1, General Controls

Product Code IXJ Grid, Radiographic
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1910
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IXJ Grid, Radiographic

Devices cleared under the same product code (IXJ) and FDA review panel - the closest regulatory comparables to K963893.
MITAYA ALUMINUM INTERSPACED X-RAY GRID
K964025 · X-Ray Accessory Corp. · Jun 1997
RADIOGRAPHIC GRID
K962338 · Unidex Group, Inc. · Jul 1996
HIGH TRANSMISSION CELLULAR (HTC) GRIDS 18X24 CM & 24X30 CM SIZES
K954294 · Thermotrex Corp. · Feb 1996
KODAK EKTASCAN SP CASSETTE
K925997 · Eastman Kodak Company · Dec 1992
AOR X-RAY ALIGMENT PAD
K837776 · Zimmer, Inc. · Aug 1983