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FDA 510(k)

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER

K-Number: K090767 · 2009-06-11

ApplicantInterventional Spine, Inc.
Decision Date2009-06-11
Product CodeMRW
DecisionUnknown

Device Summary

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Interventional Spine, Inc.. It received FDA 510(k) clearance on 2009-06-11 under 510(k) number K090767. The device is classified under product code MRW. FDA Decision: Unknown.

Frequently Asked Questions

What is the PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER?

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER is a medical device that received FDA 510(k) clearance on 2009-06-11. The listed applicant is Interventional Spine, Inc.. The 510(k) number is K090767.

When did PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER receive FDA 510(k) clearance?

PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER received FDA 510(k) clearance on 2009-06-11, under 510(k) number K090767.

Who is the listed applicant for PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER?

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

What is the FDA product code for PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER?

The FDA product code for PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER is MRW.

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Other records listing Interventional 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.

K160464Opticage(R) Expandable Interbody Fusion DeviceK132479OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00K113527OPTICAGE INTERBODY FUSION DEVICEK082795SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT

Related Devices (Code: MRW)

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.

K262618Arthrex Spine Compression FT ScrewArthrex, Inc.K261209Ion-LSurGenTec, LLCK253676CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)Providence Medical Technology, Inc.K253432DiversiVy™ Facet Screw SystemVy Spine, LLCK251714Ion-CSurGenTec, LLCK250679FFX Facet Fixation SystemSc Medica

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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