510(k) K070033— MEMOMETAL VARISATION, MODELS AV26-08, AV26-10, AV90-08 AND AV90-10

Substantially Equivalent

Memometal Technologies

Clearance details

Applicant: Memometal Technologies
Product code: Code JDR
Advisory panel: Orthopedic
Date received: 2007-01-03
Decision date: 2007-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bruz, FR

Adverse events under product code JDR

product code JDR

Injury: 726
Malfunction: 663
Other: 1
Total: 1,390

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.