MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50— 510(k) K083447

Substantially Equivalent

Memometal Technologies

FDA 510(k) clearance K083447 for MEMOMETAL ANCHORAGE BONE PLATE SYSTEM, MODELS PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50, Substantially Equivalent on 2009-02-06. Applicant: Memometal Technologies.

Clearance details

Applicant: Memometal Technologies
Product code: Code HRS
Advisory panel: Orthopedic
Date received: 2008-11-21
Decision date: 2009-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bruz, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HRS

product code HRS

Death: 27
Injury: 10,340
Malfunction: 3,328
Total: 13,695

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.