PathLoc Lumbar Interbody Fusion System

PathLoc is an expandable lumbar interbody fusion cage made from titanium alloy. Its hollow rectangular body is inserted in an unexpanded state, then raised in height using the system's…

Registry build 21.09.26

PathLoc is an expandable lumbar interbody fusion cage made from titanium alloy. Its hollow rectangular body is inserted in an unexpanded state, then raised in height using the system’s instruments.

The upper and lower surfaces have serrations for fixation against the adjacent vertebrae. PathLoc-TM is intended for transforaminal or posterior placement, with sizes and lordotic angles selected for the anatomy.

Listed Item

PathLoc – TM L25XW11, H08~12, A04

Graft and Fixation

The device accepts autogenous and/or allogeneic cancellous or corticocancellous bone graft and requires supplemental fixation. Its fusion indication covers one or two adjacent levels from L2 to S1 in skeletally mature patients.

14manufacturers in China registered for this device type
72catalogue numbers in this listing
11510(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 PathLoc Lumbar Interbody Fusion System
Listed by L&K Biomed Co., Ltd., South Korea
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, Repacker / relabeller, Manufacturer, Exporter
510(k) K213441
Record published 2022-05-16
Record revised 2025-07-14 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for PathLoc Lumbar Interbody Fusion System
Catalogue number Size Status
PT2511-0804S In distribution
PT2211-0804S In distribution
PT2511-1200 In distribution
PT2211-1212 In distribution
PT2211-1220S In distribution
PT2211-1208S In distribution
PT2211-1215S In distribution
PT2211-1204S In distribution
PT2511-1012S In distribution
PT2511-0808 In distribution
PT2211-0800S In distribution
PT2511-1000 In distribution
PT2211-1020 In distribution
PT2511-0804 In distribution
PT2511-0800 In distribution
PT2211-1008S In distribution
PT2511-0815S In distribution
PT2511-1015S In distribution
PT2511-1208 In distribution
PT2211-1015 In distribution
PT2511-0815 In distribution
PT2511-1200S In distribution
PT2211-0812S In distribution
PT2511-1012 In distribution
PT2211-1220 In distribution
PT2511-1000S In distribution
PT2511-1215 In distribution
PT2211-0804 In distribution
PT2511-0808S In distribution
PT2511-1212S In distribution
PT2211-1020S In distribution
PT2511-1212 In distribution
PT2211-1000S In distribution
PT2511-0812 In distribution
PT2511-0800S In distribution
PT2211-0808S In distribution
PT2511-1008S In distribution
PT2511-1004 In distribution
PT2511-1204 In distribution
PT2211-1204 In distribution
PT2211-1015S In distribution
PT2211-1208 In distribution
PT2211-1215 In distribution
PT2511-0820 In distribution
PT2511-1220 In distribution
PT2211-1004 In distribution
PT2511-1015 In distribution
PT2511-1220S In distribution
PT2511-0820S In distribution
PT2211-1004S In distribution
PT2511-1204S In distribution
PT2211-1000 In distribution
PT2511-1008 In distribution
PT2511-1020S In distribution
PT2211-0820S In distribution
PT2211-1200S In distribution
PT2211-0815S In distribution
PT2511-1208S In distribution
PT2211-1012 In distribution
PT2211-1200 In distribution
PT2511-1020 In distribution
PT2211-1008 In distribution
PT2211-0800 In distribution
PT2211-0808 In distribution
PT2511-0812S In distribution
PT2511-1215S In distribution
PT2211-1012S In distribution
PT2211-0820 In distribution
PT2511-1004S In distribution
PT2211-0815 In distribution
PT2211-0812 In distribution
PT2211-1212S 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
K251741 2025-07-08
K242829 2024-10-23
K231680 2023-08-24
K223474 2023-01-13
K213441 2022-03-09
K190708 2019-09-16
K181380 2018-09-11
K151140 2015-08-18
K121096 2012-07-06
K120063 2012-04-19
K110783 2011-10-24

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