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FDA 510(k)

OPTICAGE INTERBODY FUSION DEVICE

K-Number: K113527 · 2012-01-20

ApplicantInterventional Spine, Inc.
Decision Date2012-01-20
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OPTICAGE INTERBODY FUSION DEVICE 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 2012-01-20 under 510(k) number K113527. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTICAGE INTERBODY FUSION DEVICE?

OPTICAGE INTERBODY FUSION DEVICE is a medical device that received FDA 510(k) clearance on 2012-01-20. The listed applicant is Interventional Spine, Inc.. The 510(k) number is K113527.

When did OPTICAGE INTERBODY FUSION DEVICE receive FDA 510(k) clearance?

OPTICAGE INTERBODY FUSION DEVICE received FDA 510(k) clearance on 2012-01-20, under 510(k) number K113527.

Who is the listed applicant for OPTICAGE INTERBODY FUSION DEVICE?

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 OPTICAGE INTERBODY FUSION DEVICE?

The FDA product code for OPTICAGE INTERBODY FUSION DEVICE is MAX.

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 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 9080-00K090767PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZERK082795SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT

Related Devices (Code: MAX)

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.

K261049SCALA® TLSpineart SAK261430TruLift Expandable SystemLife Spine, Inc.K253011Catalyft PL Expandable Interbody SystemMedtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L Spinal SystemMedtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SySeaSpine Orthopedics CorporationK253151Fule Interbody Fusion Cage SystemBeijing Fule Science & Technology Development Co., Ltd.

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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