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FDA 510(k)

SEGMENTAL SPINAL RODS

K-Number: K851414 · 1985-06-28

ApplicantStuart
Decision Date1985-06-28
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEGMENTAL SPINAL RODS is the device name listed in this FDA 510(k) record. The listed applicant is Stuart. It received FDA 510(k) clearance on 1985-06-28 under 510(k) number K851414. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEGMENTAL SPINAL RODS?

SEGMENTAL SPINAL RODS is a medical device that received FDA 510(k) clearance on 1985-06-28. The listed applicant is Stuart. The 510(k) number is K851414.

When did SEGMENTAL SPINAL RODS receive FDA 510(k) clearance?

SEGMENTAL SPINAL RODS received FDA 510(k) clearance on 1985-06-28, under 510(k) number K851414.

Who is the listed applicant for SEGMENTAL SPINAL RODS?

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

What is the FDA product code for SEGMENTAL SPINAL RODS?

The FDA product code for SEGMENTAL SPINAL RODS is KWQ.

Related Clinical Trials

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.

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Other records listing Stuart 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.

K897141SLOT STAPLES AND ADAPTOR FOR ZIELKE SPINAL FIXATIOK890601STUART TITANIUM SURGICAL MESHK843445SACRAL BARK820034ANTERIOR DISTRACTION SYSTEM

Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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