Cleared Traditional

K830196 - CORSTREN COMPRESSION TUBE & PLATE

K830196 is an FDA 510(k) clearance for CORSTREN COMPRESSION TUBE & PLATE, manufactured by Zimmer, Inc.. The device is a Class 2 Orthopedic device with product code KTT cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K830196 · Zimmer, Inc. · Orthopedic device
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Mar 1983
Decision
64d
Days
Class 2
Risk

K830196 is an FDA 510(k) clearance for the CORSTREN COMPRESSION TUBE & PLATE. Classified as Appliance, Fixation, Nail/blade/plate Combination, Multiple Component (product code KTT), Class II - Special Controls.

Submitted by Zimmer, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 25, 1983 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3030 - 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 Zimmer, Inc. devices

FDA 510(k) Submission Details - K830196

510(k) Number K830196 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1983
Decision Date March 25, 1983
Days to Decision 64 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 122d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KTT Device Classification - Class 2, Special Controls

Product Code KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3030
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 - KTT Appliance, Fixation, Nail/blade/plate Combination, Multiple Component

All 298
Devices cleared under the same product code (KTT) and FDA review panel - the closest regulatory comparables to K830196.
T.O.D. PLATE SYSTEM
K842681 · Kirschner Medical Corp. · Sep 1984
T.O.D. PLATE SYS STERILE
K842695 · Kirschner Medical Corp. · Sep 1984
ACE/FISHER EXTERNAL FIXATOR
K842768 · Buckman Co., Inc. · Sep 1984
COMPRESSION HIP SCREW SIDE-PLATE
K823548 · Howmedica Corp. · Dec 1982
HUCKSTEP INTRAMEDULLARY NAIL
K811017 · Downs Surgical , Ltd. · May 1981
DYNAMIC HIP SCREW
K791619 · Synthes (Usa) · Aug 1979