A HOOK DRIVER— 510(k) K820660

Substantially Equivalent

Twin City Surgical, Inc.

FDA 510(k) clearance K820660 for A HOOK DRIVER, Substantially Equivalent on 1982-03-19. Applicant: Twin City Surgical, Inc..

Clearance details

Applicant: Twin City Surgical, Inc.
Product code: Code KWP
Advisory panel: Orthopedic
Date received: 1982-03-10
Decision date: 1982-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KWP

product code KWP

Death: 7
Injury: 1,539
Malfunction: 1,519
Total: 3,065

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.