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FDA 510(k)

POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS

K-Number: K121130 · 2012-06-15

ApplicantBiomet Spine
Decision Date2012-06-15
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Spine. It received FDA 510(k) clearance on 2012-06-15 under 510(k) number K121130. 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 POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS?

POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS is a medical device that received FDA 510(k) clearance on 2012-06-15. The listed applicant is Biomet Spine. The 510(k) number is K121130.

When did POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS receive FDA 510(k) clearance?

POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS received FDA 510(k) clearance on 2012-06-15, under 510(k) number K121130.

Who is the listed applicant for POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS?

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

What is the FDA product code for POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS?

The FDA product code for POLARIS SPINAL SYSTEM-BALLISTA SPINAL RODS is NKB.

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Other records listing Biomet Spine 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.

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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