SANTA CASA DISTRACTOR— 510(k) K791009

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K791009 for SANTA CASA DISTRACTOR, Substantially Equivalent on 1979-06-11. Applicant: Depuy, Inc..

Clearance details

Applicant: Depuy, Inc.
Product code: Code KWP
Advisory panel: Orthopedic
Date received: 1979-05-31
Decision date: 1979-06-11
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.