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FDA 510(k)

ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600

K-Number: K072183 · 2007-09-05

ApplicantZimmer Spine, Inc.
Decision Date2007-09-05
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Spine, Inc.. It received FDA 510(k) clearance on 2007-09-05 under 510(k) number K072183. 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 ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600?

ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 is a medical device that received FDA 510(k) clearance on 2007-09-05. The listed applicant is Zimmer Spine, Inc.. The 510(k) number is K072183.

When did ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 receive FDA 510(k) clearance?

ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 received FDA 510(k) clearance on 2007-09-05, under 510(k) number K072183.

Who is the listed applicant for ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600?

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

What is the FDA product code for ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600?

The FDA product code for ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 is NKB.

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Other records listing Zimmer Spine, Inc. 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.

K153631Zimmer Virage OCT Spinal Fixation SystemK132790INFIX ANTERIOR LUMBAR SYSTEMK133291ST360 DEGREES SPINAL FIXATION SYSTEMK133086TITLE 2 POLYAXIAL SPINAL SYSTEMK132884PATHFINDER NXT MINIMALLY INVASIVE PEDICLE SCREW SYSTEMK131980SEQUOIA PEDICLE SCREW SYSTEM INCLUDING SPEEDLINK II TRANSVERSE CONNECTOR 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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