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FDA 510(k)

IlluminOss Photodynamic Bone Stabilization System

K-Number: K233436 · 2024-01-19

Decision Date2024-01-19
Product CodeQAD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IlluminOss Photodynamic Bone Stabilization System is a medical device manufactured by Illuminoss Medical, Inc.. It received FDA 510(k) clearance on 2024-01-19 under approval number K233436. The device is classified under product code QAD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IlluminOss Photodynamic Bone Stabilization System?

IlluminOss Photodynamic Bone Stabilization System is a medical device that received FDA 510(k) clearance on 2024-01-19. It is manufactured by Illuminoss Medical, Inc.. The 510(k) number is K233436.

When was IlluminOss Photodynamic Bone Stabilization System approved by the FDA?

IlluminOss Photodynamic Bone Stabilization System received FDA 510(k) clearance on 2024-01-19, under approval number K233436.

What company makes IlluminOss Photodynamic Bone Stabilization System?

IlluminOss Photodynamic Bone Stabilization System is manufactured by Illuminoss Medical, Inc..

What is the FDA product code for IlluminOss Photodynamic Bone Stabilization System?

The FDA product code for IlluminOss Photodynamic Bone Stabilization System is QAD.

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Official Source

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