EIT Plif Cage

EIT PLIF cages are posterior lumbar interbody fusion implants made from Ti-6Al-4V ELI titanium alloy using additive manufacturing. Their design combines solid supporting structures with…

Registry build 21.09.26

EIT PLIF cages are posterior lumbar interbody fusion implants made from Ti-6Al-4V ELI titanium alloy using additive manufacturing. Their design combines solid supporting structures with porous regions and a hollow space for autogenous bone graft.

The cages restore intervertebral height as part of lumbar fusion. They are used with supplemental spinal fixation, with anterior or posterior fixation constructs selected for the procedure.

Listed Item

EIT PLIF, H 11mm, 12°, 30/11

PLIF Configuration

PLIF is the posterior-approach cage within the EIT Cellular Titanium family; the wider range has separate anterior, transforaminal and cervical designs. PLIF implants are supplied sterile in different heights, footprints and lordotic angles to accommodate patient anatomy.

14manufacturers in China registered for this device type
394catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for EIT Plif cage
Listed by EIT Emerging Implant Technologies Gmbh, Germany
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Specification developer, Manufacturer
510(k) K170503
Record published 2017-10-20
Record revised 2025-07-14 (version 6)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Distribution end date 2023-02-15

Catalogue Numbers

Catalogue numbers for EIT Plif cage
Catalogue number Size Status
PUI01622 In distribution
PUI41402 In distribution
PUI91602 In distribution
PUI31506 In distribution
PUI00806 In distribution
PUI41406 In distribution
PUI01402 In distribution
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PUI81110 In distribution
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PUI40802 In distribution
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PUI31226 In distribution
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PUI41522 In distribution
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PUI01130 In distribution
PUI40822 In distribution
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PUI01406 In distribution
PUI31322 In distribution
PUI01522 In distribution
PUI01526 In distribution
PUI31222 In distribution
PUI31422 In distribution
PUI41130 In distribution
PUI00906 In distribution
PUI41626 In distribution
PUI31310 In distribution
PUI91330 In distribution
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PUI31022 In distribution
PUI91522 In distribution
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PUI31426 In distribution

Showing 250 of 300 catalogue numbers.

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201605 2020-07-15
K183447 2019-02-04
K181644 2018-10-12
K172888 2017-12-15
K170503 2017-07-11

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of EIT Plif cage
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Depuy Spine, Inc. 510(k) number 2022-05-20 Class II Labeling Change Control Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton 61 units
Depuy Spine, Inc. 510(k) number 2022-05-20 Class II Labeling Change Control Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton 46 units

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer