ADULT WALKING HEEL PRODUCT NO. 4183-130— 510(k) K873716

Substantially Equivalent

Martin Medical

FDA 510(k) clearance K873716 for ADULT WALKING HEEL PRODUCT NO. 4183-130, Substantially Equivalent on 1987-10-02. Applicant: Martin Medical.

Clearance details

Applicant: Martin Medical
Product code: Code LDF
Advisory panel: Cardiovascular
Date received: 1987-09-15
Decision date: 1987-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Desoto, KS, US

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Adverse events under product code LDF

product code LDF

Death: 19
Injury: 188
Malfunction: 694
Other: 1
Total: 902

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.