ELEOSx Limb Salvage System— 510(k) DEN210058

Unknown

Onkos Surgical

FDA 510(k) clearance DEN210058 for ELEOSx Limb Salvage System, Unknown on 2024-04-05. Applicant: Onkos Surgical. Device class: 2.

Clearance details

Applicant: Onkos Surgical
Product code: Code QZZ
Device class: Class 2
Regulation: 21 CFR 888.3900
Advisory panel: Orthopedic
Date received: 2021-12-30
Decision date: 2024-04-05
Decision: Unknown
Clearance type: Direct
Location: Parsippany, NJ, US

View on FDA.gov ↗

Recent devices under product code QZZ

More clearances from Onkos Surgical

K212815 — My3D® Personalized Pelvic Reconstruction2022-07-06
K211677 — ELEOS Limb Salvage System2021-07-28
K203815 — ELEOS Limb Salvage System with BioGrip2021-06-09
K203588 — ELEOS Limb Salvage System2021-02-05
K203090 — ELEOS Limb Salvage System featuring BIOGRIP2020-12-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.