THE ORIGINAL LEINBACH PLATFORM TOTAL HIP— 510(k) K820755

Name: FDA 510(k) clearance K820755
Creator: U.S. Food and Drug Administration
Published: 1982-06-10

Substantially Equivalent

Allo Pro Corp.

FDA 510(k) clearance K820755 for THE ORIGINAL LEINBACH PLATFORM TOTAL HIP, Substantially Equivalent on 1982-06-10. Applicant: Allo Pro Corp.. Device class: 2.

Clearance details

Applicant: Allo Pro Corp.
Product code: Code KWL
Device class: Class 2
Regulation: 21 CFR 888.3360
Advisory panel: Orthopedic
Date received: 1982-03-19
Decision date: 1982-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K242865 — Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer2025-06-12

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Adverse events under product code KWL

product code KWL

Injury: 523
Total: 523

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.