CEMENT AND BONE REMOVAL KIT— 510(k) K961759

Name: FDA 510(k) clearance K961759
Creator: U.S. Food and Drug Administration
Published: 1996-06-13

Substantially Equivalent

Maillefer Instruments S.A.

FDA 510(k) clearance K961759 for CEMENT AND BONE REMOVAL KIT, Substantially Equivalent on 1996-06-13. Applicant: Maillefer Instruments S.A.. Device class: 1.

Clearance details

Applicant: Maillefer Instruments S.A.
Product code: Code HWE
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1996-05-07
Decision date: 1996-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moorpark, CA, US

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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.