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FDA 510(k)

Xultan 5.5 Pedicle Screw System

K-Number: K170108 · 2017-05-02

ApplicantMet One Technologies
Decision Date2017-05-02
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Xultan 5.5 Pedicle Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Met One Technologies. It received FDA 510(k) clearance on 2017-05-02 under 510(k) number K170108. 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 Xultan 5.5 Pedicle Screw System?

Xultan 5.5 Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2017-05-02. The listed applicant is Met One Technologies. The 510(k) number is K170108.

When did Xultan 5.5 Pedicle Screw System receive FDA 510(k) clearance?

Xultan 5.5 Pedicle Screw System received FDA 510(k) clearance on 2017-05-02, under 510(k) number K170108.

Who is the listed applicant for Xultan 5.5 Pedicle Screw System?

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

What is the FDA product code for Xultan 5.5 Pedicle Screw System?

The FDA product code for Xultan 5.5 Pedicle Screw System is NKB.

Other records listing Met One Technologies as applicant

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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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