Cleared Traditional

K791919 - BAC JAC

K791919 is the FDA 510(k) clearance for BAC JAC by Haggin Industries, Inc.. It is a Class 1 Neurology device (product code HST) cleared through the Traditional 510(k) pathway after a 9-day FDA review.

K791919 · Haggin Industries, Inc. · Neurology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1979
Decision
9d
Days
Class 1
Risk

K791919 is an FDA 510(k) clearance for the BAC JAC. Classified as Apparatus, Traction, Non-powered (product code HST), Class I - General Controls.

Submitted by Haggin Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 4, 1979 after a review of 9 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 888.5850 - 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 Haggin Industries, Inc. devices

Submission Details

510(k) Number K791919 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 25, 1979
Decision Date October 04, 1979
Days to Decision 9 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
139d faster than avg
Panel avg: 148d · This submission: 9d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code HST Apparatus, Traction, Non-powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.5850
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 - HST Apparatus, Traction, Non-powered

All 14
Devices cleared under the same product code (HST) and FDA review panel - the closest regulatory comparables to K791919.
FOREARM REDUCTION UNIT
K823392 · Orthopedic Systems, Inc. · Nov 1982
TENSOPLAST SKIN TRACTION KIT
K820612 · Smith & Nephew, Inc. · Mar 1982
UPPER EXTREMITY TRACTION DEVICE
K803021 · Orthopedic Systems, Inc. · Dec 1980
OCTAGONAL ALUMINUM FRAMING SYSTEM
K790729 · Orthopedic Systems, Inc. · May 1979
TRACTION UNITS
K780228 · Biomet, Inc. · Feb 1978
TRACTION WEIGHT BAGS
K780233 · Biomet, Inc. · Feb 1978