Cleared Traditional

K960482 - K-WIRE

K960482 is an FDA 510(k) clearance for K-WIRE, manufactured by American Medical Specialties, Inc.. The device is a Class 2 Orthopedic device with product code HTY cleared through the Traditional 510(k) pathway after a 67-day FDA review.

K960482 · American Medical Specialties, Inc. · Orthopedic device
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Apr 1996
Decision
67d
Days
Class 2
Risk

K960482 is an FDA 510(k) clearance for the K-WIRE. Classified as Pin, Fixation, Smooth (product code HTY), Class II - Special Controls.

Submitted by American Medical Specialties, Inc. (Norcross, US). The FDA issued a Cleared decision on April 9, 1996 after a review of 67 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 American Medical Specialties, Inc. devices

FDA 510(k) Submission Details - K960482

510(k) Number K960482 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 02, 1996
Decision Date April 09, 1996
Days to Decision 67 days
Submission Type Traditional
Review Panel Orthopedic (OR)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
55d faster than avg
Panel avg: 122d · This submission: 67d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HTY Device Classification - Class 2, Special Controls

Product Code HTY Pin, Fixation, Smooth
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 - HTY Pin, Fixation, Smooth

All 159
Devices cleared under the same product code (HTY) and FDA review panel - the closest regulatory comparables to K960482.
RMS K-WIRE
K963367 · Rms Div. · Oct 1996
KIRSCHNER WIRE (K-WIRE) AND STEINMANN PIN
K961522 · Synvasive Technology, Inc. · Sep 1996
NANCY NAIL
K960642 · Landos, Inc. · May 1996
STEINMAN PIN
K960483 · American Medical Specialties, Inc. · Apr 1996
STERILE KIRSCHNER WIRES AND STEINMANN PINS
K960385 · Depuy, Inc. · Mar 1996
HOWMEDICA BIOABSORBABLE PIN
K955806 · Howmedica, Inc. · Feb 1996