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FDA 510(k)

PressON Spinal Fixation System

K-Number: K253331 · 2025-10-14

ApplicantNexus Spine
Decision Date2025-10-14
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PressON Spinal Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Nexus Spine. It received FDA 510(k) clearance on 2025-10-14 under 510(k) number K253331. 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 PressON Spinal Fixation System?

PressON Spinal Fixation System is a medical device that received FDA 510(k) clearance on 2025-10-14. The listed applicant is Nexus Spine. The 510(k) number is K253331.

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

PressON Spinal Fixation System received FDA 510(k) clearance on 2025-10-14, under 510(k) number K253331.

Who is the listed applicant for PressON Spinal Fixation System?

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

What is the FDA product code for PressON Spinal Fixation System?

The FDA product code for PressON Spinal Fixation System is NKB.

Other records listing Nexus Spine 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.

K261279DeltaNEC Interbody SystemK243934Stable-L Lumbar Interbody SystemK241467Stable-C Interbody SystemK233375Tranquil-L Interbody SystemK240416Tranquil-C Interbody SystemK233234PressON Spinal Fixation System

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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.

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