Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Duet™ Spinal Fixation System

K-Number: K253169 · 2026-02-23

ApplicantBox Spine, LLC
Decision Date2026-02-23
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Duet™ Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Box Spine, LLC. It received FDA 510(k) clearance on 2026-02-23 under 510(k) number K253169. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Duet™ Spinal Fixation System?

Duet™ Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2026-02-23. The listed applicant is Box Spine, LLC. The 510(k) number is K253169.

When did Duet™ Spinal Fixation System receive FDA 510(k) clearance?

Duet™ Spinal Fixation System received FDA 510(k) clearance on 2026-02-23, under 510(k) number K253169.

Who is the listed applicant for Duet™ Spinal Fixation System?

The FDA 510(k) record lists Box Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Duet™ Spinal Fixation System?

The FDA product code for Duet™ Spinal Fixation System is NKB.

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.

K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.K253943Tiger 2 SystemZavation Medical Products, LLCK261284Invictus® Small Stature Spinal Fixation System; Invictus® 2.0 Spinal Fixation SystemAlphatec Spine, Inc.K253802KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK253045“Socko” Vimax Spinal Fixation SystemSocko Medical Co., Ltd.K251251ChanPin Pedicle Screw Spinal SystemChanpin Medtak Co., Ltd.

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.

↑