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FDA 510(k)

CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE

K-Number: K121254 · 2013-01-11

ApplicantCamber Spine Technologies
Decision Date2013-01-11
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE is the device name listed in this FDA 510(k) record. The listed applicant is Camber Spine Technologies. It received FDA 510(k) clearance on 2013-01-11 under 510(k) number K121254. 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 CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE?

CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE is a medical device that received FDA 510(k) clearance on 2013-01-11. The listed applicant is Camber Spine Technologies. The 510(k) number is K121254.

When did CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE receive FDA 510(k) clearance?

CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE received FDA 510(k) clearance on 2013-01-11, under 510(k) number K121254.

Who is the listed applicant for CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE?

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

What is the FDA product code for CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE?

The FDA product code for CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE is MAX.

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Other records listing Camber Spine Technologies as applicant

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K234077SPIRA® Anterior Lumbar SpacersK233972Camber Sacroiliac (SI) Fixation SystemK230942SPIRA® Posterior Lumbar SpacersK221324ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)K223837SPIRA®-C Integrated Fixation SystemK220038Camber Spine Navigation System

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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

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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