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FDA 510(k)

HC Biologics Osteopoint Spinal Fixation System

K-Number: K250092 · 2025-03-27

Decision Date2025-03-27
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HC Biologics Osteopoint Spinal Fixation System is a medical device manufactured by HC Biologics, LLC. It received FDA 510(k) clearance on 2025-03-27 under approval number K250092. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HC Biologics Osteopoint Spinal Fixation System?

HC Biologics Osteopoint Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2025-03-27. It is manufactured by HC Biologics, LLC. The 510(k) number is K250092.

When was HC Biologics Osteopoint Spinal Fixation System approved by the FDA?

HC Biologics Osteopoint Spinal Fixation System received FDA 510(k) clearance on 2025-03-27, under approval number K250092.

What company makes HC Biologics Osteopoint Spinal Fixation System?

HC Biologics Osteopoint Spinal Fixation System is manufactured by HC Biologics, LLC.

What is the FDA product code for HC Biologics Osteopoint Spinal Fixation System?

The FDA product code for HC Biologics Osteopoint Spinal Fixation System is NKB.

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Official Source

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