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FDA 510(k)

VIPER SYSTEMS

K-Number: K111571 · 2011-07-06

ApplicantJohnson & Johnson
Decision Date2011-07-06
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VIPER SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson. It received FDA 510(k) clearance on 2011-07-06 under 510(k) number K111571. 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 VIPER SYSTEMS?

VIPER SYSTEMS is a medical device that received FDA 510(k) clearance on 2011-07-06. The listed applicant is Johnson & Johnson. The 510(k) number is K111571.

When did VIPER SYSTEMS receive FDA 510(k) clearance?

VIPER SYSTEMS received FDA 510(k) clearance on 2011-07-06, under 510(k) number K111571.

Who is the listed applicant for VIPER SYSTEMS?

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

What is the FDA product code for VIPER SYSTEMS?

The FDA product code for VIPER SYSTEMS is NKB.

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Other records listing Johnson & Johnson 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.

K113273SPOTLIGHT ACCESS SYSTEMK112913SPOTLIGHT ACCESS SYSTEMK113348COUGAR SYSTEMK110551EXPEDIUM SPINE SYSTEMK110694CONCORDE BULLET SPINAL SYSTEMK110454COUGAR LS LATERAL CAGE 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.

K252139Kentrospine Viktr-MIS® Pedicle screw systemRivarp Medical Pvt., Ltd.K262067iFuse Granite Onyx™ Implant SystemSI-BONE, Inc.K262091FRAXION Spinal Fixation SystemOrtler Global Tibbi Gerecler Anonim SirketiK262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix MedicalK262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.OK260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ 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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