Cleared Traditional

K871911 - THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION

K871911 is an FDA 510(k) clearance for THE F SPOON HAND HELD FLUOROSCOPIC COMP..., manufactured by F. Spoon Co.. The device is a Class 2 Radiology device with product code JAA cleared through the Traditional 510(k) pathway after a 11-day FDA review.

K871911 · F. Spoon Co. · Radiology device
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May 1987
Decision
11d
Days
Class 2
Risk

K871911 is an FDA 510(k) clearance for the THE F SPOON HAND HELD FLUOROSCOPIC COMPRESSION. Classified as System, X-ray, Fluoroscopic, Image-intensified (product code JAA), Class II - Special Controls.

Submitted by F. Spoon Co. (Dover, US). The FDA issued a Cleared decision on May 29, 1987 after a review of 11 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - 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 F. Spoon Co. devices

FDA 510(k) Submission Details - K871911

510(k) Number K871911 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 18, 1987
Decision Date May 29, 1987
Days to Decision 11 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
96d faster than avg
Panel avg: 107d · This submission: 11d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAA Device Classification - Class 2, Special Controls

Product Code JAA System, X-ray, Fluoroscopic, Image-intensified
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
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 Radiology devices follow this clearance model.

Regulatory Peers - JAA System, X-ray, Fluoroscopic, Image-intensified

All 195
Devices cleared under the same product code (JAA) and FDA review panel - the closest regulatory comparables to K871911.
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