BethaLoc® stem cementless HA— 510(k) K223103

Substantially Equivalent

Implantcast GmbH

FDA 510(k) clearance K223103 for BethaLoc® stem cementless HA, Substantially Equivalent on 2023-06-20. Applicant: Implantcast GmbH.

Clearance details

Applicant: Implantcast GmbH
Product code: Code LZO
Advisory panel: Orthopedic
Date received: 2022-09-30
Decision date: 2023-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Buxtehude, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code LZO

product code LZO

Death: 17
Injury: 12,942
Malfunction: 1,756
Total: 14,715

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.