TAVERNETTI-TENNANT— 510(k) K760744

Name: FDA 510(k) clearance K760744
Creator: U.S. Food and Drug Administration
Published: 1976-10-07

Substantially Equivalent

Cutter Laboratories, Inc.

FDA 510(k) clearance K760744 for TAVERNETTI-TENNANT, Substantially Equivalent on 1976-10-07. Applicant: Cutter Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Cutter Laboratories, Inc.
Product code: Code HRY
Device class: Class 2
Regulation: 21 CFR 888.3530
Advisory panel: Orthopedic
Date received: 1976-09-30
Decision date: 1976-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HRY

product code HRY

Injury: 1,551
Malfunction: 2,753
Total: 4,304

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.