GRAFTOLOGER PGH & ACL RECONSTRUCTION INSTRUMENT SET— 510(k) K952543

Substantially Equivalent

Neoligaments, Ltd.

FDA 510(k) clearance K952543 for GRAFTOLOGER PGH & ACL RECONSTRUCTION INSTRUMENT SET, Substantially Equivalent on 1995-06-22. Applicant: Neoligaments, Ltd..

Clearance details

Applicant: Neoligaments, Ltd.
Product code: Code HWE
Advisory panel: General, Plastic Surgery
Date received: 1995-05-18
Decision date: 1995-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leeds, GB

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Adverse events under product code HWE

product code HWE

Death: 4
Injury: 448
Malfunction: 19,856
Other: 2
Total: 20,310

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.