ACUFEX INTERFERENCE SCREW, STERILE— 510(k) K895711

Substantially Equivalent

Acufex Microsurgical, Inc.

FDA 510(k) clearance K895711 for ACUFEX INTERFERENCE SCREW, STERILE, Substantially Equivalent on 1990-01-09. Applicant: Acufex Microsurgical, Inc..

Clearance details

Applicant: Acufex Microsurgical, Inc.
Product code: Code HWC
Advisory panel: Orthopedic
Date received: 1989-09-25
Decision date: 1990-01-09
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.