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FDA 510(k)

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM

K-Number: K102020 · 2010-09-01

ApplicantSpinefrontier, Inc.
Decision Date2010-09-01
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Spinefrontier, Inc.. It received FDA 510(k) clearance on 2010-09-01 under 510(k) number K102020. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEGA SPAN SPINOUS PROCESS PLATE SYSTEM?

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-09-01. The listed applicant is Spinefrontier, Inc.. The 510(k) number is K102020.

When did VEGA SPAN SPINOUS PROCESS PLATE SYSTEM receive FDA 510(k) clearance?

VEGA SPAN SPINOUS PROCESS PLATE SYSTEM received FDA 510(k) clearance on 2010-09-01, under 510(k) number K102020.

Who is the listed applicant for VEGA SPAN SPINOUS PROCESS PLATE SYSTEM?

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

What is the FDA product code for VEGA SPAN SPINOUS PROCESS PLATE SYSTEM?

The FDA product code for VEGA SPAN SPINOUS PROCESS PLATE SYSTEM is KWP.

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Other records listing Spinefrontier, 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.

K193106SpineFrontier Lumbar Interbody Fusion Device SystemK172484A-CIFT SoloFuseK132740SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEMK123164SPINEFRONTIER PEDFUSE PEDICLE SCREW SYSTEMK121060SPINE FRONTIER INDUS ACP SYSTEMK113518ARENA-C CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

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Related Devices (Code: KWP)

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.

K133094CERTEX OCT SPINAL IMPLANT SYSTEMX-Spine Systems, Inc.K132504TIGER OCCIPITAL-CERVICAL-THORACIC SPINAL FIXATION SYSTEMCorelink, LLCK132900MARAUDER CERVICAL-THORACIC SPINAL FIXATION SYSTEMIntelligent Implant Systems, LLCK131427LOTUSSpinal Elements, Inc.K132332MOUNTAINEER OCT SPINAL SYSTEMMedos International SARLK131156LANX SPINAL FIXATION SYSTEMLanx, Inc.

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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