MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)— 510(k) K102072

Substantially Equivalent

Memometal Technologies

FDA 510(k) clearance K102072 for MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE), Substantially Equivalent on 2010-11-03. Applicant: Memometal Technologies.

Clearance details

Applicant: Memometal Technologies
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 2010-07-23
Decision date: 2010-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bruz, FR

Download summary PDF View on FDA.gov ↗

Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.