RMS K-WIRE— 510(k) K963367

Name: FDA 510(k) clearance K963367
Creator: U.S. Food and Drug Administration
Published: 1996-10-30

Substantially Equivalent

Rms Div.

FDA 510(k) clearance K963367 for RMS K-WIRE, Substantially Equivalent on 1996-10-30. Applicant: Rms Div.. Device class: 2.

Clearance details

Applicant: Rms Div.
Product code: Code HTY
Device class: Class 2
Regulation: 21 CFR 888.3040
Advisory panel: Orthopedic
Date received: 1996-08-27
Decision date: 1996-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.