Cleared Traditional

K803166 - DOUBLE BALL JOINT

K803166 is an FDA 510(k) clearance for DOUBLE BALL JOINT, manufactured by Howmedica Corp.. The device is a Class 2 Orthopedic device with product code JEC cleared through the Traditional 510(k) pathway after a 25-day FDA review.

K803166 · Howmedica Corp. · Orthopedic device
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Jan 1981
Decision
25d
Days
Class 2
Risk

K803166 is an FDA 510(k) clearance for the DOUBLE BALL JOINT. Classified as Component, Traction, Invasive (product code JEC), Class II - Special Controls.

Submitted by Howmedica Corp. (Walker, US). The FDA issued a Cleared decision on January 9, 1981 after a review of 25 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3040 - the FDA orthopedic device regulatory 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 Howmedica Corp. devices

FDA 510(k) Submission Details - K803166

510(k) Number K803166 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1980
Decision Date January 09, 1981
Days to Decision 25 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 122d · This submission: 25d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JEC Device Classification - Class 2, Special Controls

Product Code JEC Component, Traction, Invasive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3040
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 Orthopedic devices follow this clearance model.

Regulatory Peers - JEC Component, Traction, Invasive

All 53
Devices cleared under the same product code (JEC) and FDA review panel - the closest regulatory comparables to K803166.
OXFORD MARK 2 EXTERNAL FIXATOR
K833114 · Johnson & Johnson Professionals, Inc. · Oct 1983
ORTHOFIX
K831576 · Electro-Biology, Inc. · Jun 1983
COLLES FRACTURE FRAME
K830154 · Richard'S Medical Equip., Inc. · Feb 1983
EXTERNAL FIXATION SYSTEM
K802722 · Howmedica Corp. · Nov 1980
EXTENDED BALLJOINT GRIP
K802723 · Howmedica Corp. · Nov 1980
HOFFMAN LEG LENGTHENING DEVICE
K802776 · Howmedica Corp. · Nov 1980