NEX-D2 Posterior Fixation System
K-Number: K190981 · 2020-01-15
Device Summary
Frequently Asked Questions
What is the NEX-D2 Posterior Fixation System?
NEX-D2 Posterior Fixation System is a medical device that received FDA 510(k) clearance on 2020-01-15. The listed applicant is Next Orthosurgical. The 510(k) number is K190981.
When did NEX-D2 Posterior Fixation System receive FDA 510(k) clearance?
NEX-D2 Posterior Fixation System received FDA 510(k) clearance on 2020-01-15, under 510(k) number K190981.
Who is the listed applicant for NEX-D2 Posterior Fixation System?
The FDA 510(k) record lists Next Orthosurgical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEX-D2 Posterior Fixation System?
The FDA product code for NEX-D2 Posterior Fixation System is NKB.
Other records listing Next Orthosurgical 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: NKB)
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.