510(k) K760650— RETRACTOR, GERBODE STERNAL

Substantially Equivalent

Dilling Co.

Clearance details

Applicant: Dilling Co.
Product code: Code GAP
Advisory panel: General, Plastic Surgery
Date received: 1976-09-15
Decision date: 1976-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Adverse events under product code GAP

product code GAP

Death: 3
Injury: 491
Malfunction: 2,253
Total: 2,747

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.