SILIMED GLUTEAL IMPLANT— 510(k) K974482

Substantially Equivalent

Silimed, LLC

FDA 510(k) clearance K974482 for SILIMED GLUTEAL IMPLANT, Substantially Equivalent on 1998-02-24. Applicant: Silimed, LLC.

Clearance details

Applicant: Silimed, LLC
Product code: Code MIB
Advisory panel: Ear, Nose, Throat
Date received: 1997-11-26
Decision date: 1998-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

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Adverse events under product code MIB

product code MIB

Injury: 146
Total: 146

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.