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FDA 510(k)

MLP Special Locking Bone Plate System

K-Number: K181843 · 2019-03-04

ApplicantMaxxion Medical, LLC / Baumer SA
Decision Date2019-03-04
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MLP Special Locking Bone Plate System is a medical device manufactured by Maxxion Medical, LLC / Baumer SA. It received FDA 510(k) clearance on 2019-03-04 under approval number K181843. 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 MLP Special Locking Bone Plate System?

MLP Special Locking Bone Plate System is a medical device that received FDA 510(k) clearance on 2019-03-04. It is manufactured by Maxxion Medical, LLC / Baumer SA. The 510(k) number is K181843.

When was MLP Special Locking Bone Plate System approved by the FDA?

MLP Special Locking Bone Plate System received FDA 510(k) clearance on 2019-03-04, under approval number K181843.

What company makes MLP Special Locking Bone Plate System?

MLP Special Locking Bone Plate System is manufactured by Maxxion Medical, LLC / Baumer SA.

What is the FDA product code for MLP Special Locking Bone Plate System?

The FDA product code for MLP Special Locking Bone Plate System is 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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