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FDA 510(k)

OIC Small / Mini Fragment Plate System

K-Number: K242995 · 2024-10-23

ApplicantThe Orthopaedic Implant Company
Decision Date2024-10-23
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OIC Small / Mini Fragment Plate System is a medical device manufactured by The Orthopaedic Implant Company. It received FDA 510(k) clearance on 2024-10-23 under approval number K242995. 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 OIC Small / Mini Fragment Plate System?

OIC Small / Mini Fragment Plate System is a medical device that received FDA 510(k) clearance on 2024-10-23. It is manufactured by The Orthopaedic Implant Company. The 510(k) number is K242995.

When was OIC Small / Mini Fragment Plate System approved by the FDA?

OIC Small / Mini Fragment Plate System received FDA 510(k) clearance on 2024-10-23, under approval number K242995.

What company makes OIC Small / Mini Fragment Plate System?

OIC Small / Mini Fragment Plate System is manufactured by The Orthopaedic Implant Company.

What is the FDA product code for OIC Small / Mini Fragment Plate System?

The FDA product code for OIC Small / Mini Fragment Plate System is HRS.

Related Clinical Trials

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Related PubMed Literature

PMID: 42168293 Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling. Scientific reports (2026)

Other Devices by The Orthopaedic Implant Company

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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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