dynaMX™ Compression Plate
K-Number: K161303 · 2017-01-26
Device Summary
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. The listed applicant is Mx Orthopedics, Corp.. The 510(k) number is K161303.
When did dynaMX™ Compression Plate receive FDA 510(k) clearance?
dynaMX™ Compression Plate received FDA 510(k) clearance on 2017-01-26, under 510(k) number K161303.
Who is the listed applicant for dynaMX™ Compression Plate?
The FDA 510(k) record lists Mx Orthopedics, Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for dynaMX™ Compression Plate?
The FDA product code for dynaMX™ Compression Plate is HRS.
Other records listing Mx Orthopedics, Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.