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FDA 510(k)

Protean Fragment Plating System

K-Number: K241815 · 2024-09-26

ApplicantSkeletal Dynamics, Inc.
Decision Date2024-09-26
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Protean Fragment Plating System is a medical device manufactured by Skeletal Dynamics, Inc.. It received FDA 510(k) clearance on 2024-09-26 under approval number K241815. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Protean Fragment Plating System?

Protean Fragment Plating System is a medical device that received FDA 510(k) clearance on 2024-09-26. It is manufactured by Skeletal Dynamics, Inc.. The 510(k) number is K241815.

When was Protean Fragment Plating System approved by the FDA?

Protean Fragment Plating System received FDA 510(k) clearance on 2024-09-26, under approval number K241815.

What company makes Protean Fragment Plating System?

Protean Fragment Plating System is manufactured by Skeletal Dynamics, Inc..

What is the FDA product code for Protean Fragment Plating System?

The FDA product code for Protean Fragment Plating System is HRS.

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Related Devices (Code: HRS)

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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.

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