BLADE PLATE— 510(k) K905352

Name: FDA 510(k) clearance K905352
Creator: U.S. Food and Drug Administration
Published: 1990-12-11

Substantially Equivalent

O'Tec Corp.

FDA 510(k) clearance K905352 for BLADE PLATE, Substantially Equivalent on 1990-12-11. Applicant: O'Tec Corp.. Device class: 2.

Clearance details

Applicant: O'Tec Corp.
Product code: Code KTT
Device class: Class 2
Regulation: 21 CFR 888.3030
Advisory panel: Orthopedic
Date received: 1990-11-28
Decision date: 1990-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Memphis, TN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KTT

product code KTT

Death: 11
Injury: 3,097
Malfunction: 1,261
Total: 4,369

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.