EIT Plif Trial

Trial, H: 11 mm, 8°, 30/11

Registry build 21.09.26
14manufacturers in China registered for this device type
103catalogue 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 Trial
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 2018-09-27
Record revised 2019-02-07 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number, manufacturing date

Catalogue Numbers

Catalogue numbers for EIT Plif Trial
Catalogue number Size Status
PET81130 In distribution
PET91306 In distribution
PET81310 In distribution
PET20930 In distribution
PET91010 In distribution
PET31206 In distribution
PET91006 In distribution
PET81510 In distribution
PET61410 In distribution
PET00810 In distribution
PET80810 In distribution
PET91610 In distribution
PET21230 In distribution
PET31106 In distribution
PET60910 In distribution
PET61430 In distribution
PET21010 In distribution
PET21130 In distribution
PET61210 In distribution
PET91406 In distribution
PET60930 In distribution
PET01310 In distribution
PET31510 In distribution
PET81030 In distribution
PET91510 In distribution
PET01210 In distribution
PET61110 In distribution
PET61510 In distribution
PET20710 In distribution
PET01630 In distribution
PET60810 In distribution
PET31610 In distribution
PET81410 In distribution
PET61530 In distribution
PET61230 In distribution
PET21110 In distribution
PET21530 In distribution
PET20830 In distribution
PET91310 In distribution
PET21210 In distribution
PET31506 In distribution
PET81230 In distribution
PET21410 In distribution
PET20810 In distribution
PET01330 In distribution
PET61610 In distribution
PET91106 In distribution
PET20730 In distribution
PET80830 In distribution
PET81210 In distribution
PET80910 In distribution
PET30906 In distribution
PET01410 In distribution
PET91410 In distribution
PET61010 In distribution
PET61330 In distribution
PET91206 In distribution
PET01530 In distribution
PET20910 In distribution
PET01110 In distribution
PET21430 In distribution
PET21030 In distribution
PET21330 In distribution
PET21610 In distribution
PET21510 In distribution
PET31210 In distribution
PET31006 In distribution
PET31110 In distribution
PET31310 In distribution
PET61030 In distribution
PET01030 In distribution
PET01010 In distribution
PET61130 In distribution
PET60830 In distribution
PET01610 In distribution
PET91506 In distribution
PET30910 In distribution
PET81430 In distribution
PET31406 In distribution
PET80930 In distribution
PET31306 In distribution
PET91210 In distribution
PET01510 In distribution
PET01430 In distribution
PET61310 In distribution
PET81330 In distribution
PET91606 In distribution
PET81010 In distribution
PET00930 In distribution
PET01230 In distribution
PET21630 In distribution
PET81630 In distribution
PET31010 In distribution
PET00830 In distribution
PET01130 In distribution
PET00710 In distribution
PET81110 In distribution
PET00730 In distribution
PET61630 In distribution
PET31410 In distribution
PET21310 In distribution
PET81530 In distribution
PET31606 In distribution

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 Trial
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