Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ELEOS Limb Salvage System featuring BIOGRIP

K-Number: K203090 · 2020-12-11

Decision Date2020-12-11
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ELEOS Limb Salvage System featuring BIOGRIP is a medical device manufactured by Onkos Surgical. It received FDA 510(k) clearance on 2020-12-11 under approval number K203090. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELEOS Limb Salvage System featuring BIOGRIP?

ELEOS Limb Salvage System featuring BIOGRIP is a medical device that received FDA 510(k) clearance on 2020-12-11. It is manufactured by Onkos Surgical. The 510(k) number is K203090.

When was ELEOS Limb Salvage System featuring BIOGRIP approved by the FDA?

ELEOS Limb Salvage System featuring BIOGRIP received FDA 510(k) clearance on 2020-12-11, under approval number K203090.

What company makes ELEOS Limb Salvage System featuring BIOGRIP?

ELEOS Limb Salvage System featuring BIOGRIP is manufactured by Onkos Surgical.

What is the FDA product code for ELEOS Limb Salvage System featuring BIOGRIP?

The FDA product code for ELEOS Limb Salvage System featuring BIOGRIP is JDI.

Other Devices by Onkos Surgical

Related Devices (Code: JDI)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.