dynaMX Compression Plate
K-Number: K161303 · 2017-01-26
ApplicantMx Orthopedics, Corp.
Decision Date2017-01-26
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
dynaMX Compression Plate is a medical device manufactured by Mx Orthopedics, Corp.. It received FDA 510(k) clearance on 2017-01-26 under approval number K161303. 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 dynaMX Compression Plate?
dynaMX Compression Plate is a medical device that received FDA 510(k) clearance on 2017-01-26. It is manufactured by Mx Orthopedics, Corp.. The 510(k) number is K161303.
When was dynaMX Compression Plate approved by the FDA?
dynaMX Compression Plate received FDA 510(k) clearance on 2017-01-26, under approval number K161303.
What company makes dynaMX Compression Plate?
dynaMX Compression Plate is manufactured by Mx Orthopedics, Corp..
What is the FDA product code for dynaMX Compression Plate?
The FDA product code for dynaMX Compression Plate 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.