ACUFEX STERILE CANNULATED INTERFERENCE SCREW;— 510(k) K900132

Substantially Equivalent

Acufex Microsurgical, Inc.

FDA 510(k) clearance K900132 for ACUFEX STERILE CANNULATED INTERFERENCE SCREW;, Substantially Equivalent on 1990-03-28. Applicant: Acufex Microsurgical, Inc..

Clearance details

Applicant: Acufex Microsurgical, Inc.
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 1990-01-10
Decision date: 1990-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwood, MA, US

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Adverse events under product code HWC

product code HWC

Death: 20
Injury: 15,910
Malfunction: 8,192
Other: 1
Total: 24,123

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.