Lumbar Interbody Fusion System (Ollif)
Lumbar Interbody Fusion System (OLLIF) Handheld Microscope - Light Guide Alignment Sleeve
14manufacturers in China registered for this device type
71catalogue numbers in this listing
1510(k) clearance
1recall
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.
| 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
| Listed by | Advanced Research Medical, United States |
|---|---|
| FDA product code | MAX |
| Device type | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3080 |
| Establishment | Manufacturer |
| 510(k) | K173947 |
| Record published | 2019-12-16 |
| Record revised | 2025-07-14 (version 8) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, manufacturing date |
| Packaging | Pack of 10, pack of 25, pack of 100 |
| Sizes | Length 2 to 33 mm; height 8 to 15 mm; width 9.5 to 10 mm; guidewire diameter 1.4 mm; length 18 in |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 01-3015 | Width 9.5 mm | In distribution |
| 01-100 | In distribution | |
| 01-3010 | Width 9.5 mm | In distribution |
| 01-3310 | Width 9.5 mm | In distribution |
| 01-14-2 | In distribution | |
| 01-C2 | In distribution | |
| 01-2713 | Width 9.5 mm | In distribution |
| 01-11 | In distribution | |
| 01-3308 | Width 9.5 mm | In distribution |
| 01-08 | In distribution | |
| 01-2000 | In distribution | |
| 01-2709 | Height 9.5 mm | In distribution |
| 01-2711 | Width 9.5 mm | In distribution |
| 01-P2 | In distribution | |
| 01-3011 | Height 11 mm | In distribution |
| 01-10 | In distribution | |
| 01-14-3 | In distribution | |
| 01-07 | In distribution | |
| 01-01 | In distribution | |
| 01-06-2 | In distribution | |
| 01-T3 | In distribution | |
| 01-00-1 | In distribution | |
| 01-3312 | Width 9.5 mm | In distribution |
| 01-06-4 | In distribution | |
| 01-3311 | Width 9.5 mm | In distribution |
| 01-2715 | Width 9.5 mm | In distribution |
| 01-P3 | In distribution | |
| 01-3315 | Height 15 mm | In distribution |
| 01-09 | In distribution | |
| 01-B1 | In distribution | |
| 01-06-3 | In distribution | |
| 01-15 | In distribution | |
| 01-2712 | Height 12 mm | In distribution |
| 01-3012 | Width 9.5 mm | In distribution |
| O-3300 | In distribution | |
| 01-C4 | In distribution | |
| 01-14-6 | In distribution | |
| 01-02 | In distribution | |
| 01-04-2 | In distribution | |
| 01-12 | In distribution | |
| 01-3008 | Width 9.5 mm | In distribution |
| 01-101 | In distribution | |
| 01-3313 | Width 9.5 mm | In distribution |
| 01-2714 | Width 9.5 mm | In distribution |
| 01-14-4 | In distribution | |
| 01-T1 | In distribution | |
| 01-9080-18U | Guidewire Diameter 1.4 mm | In distribution |
| 01-3309 | Length 33 mm | In distribution |
| 01-04-1 | In distribution | |
| 01-C3 | In distribution | |
| 01-2708 | Width 9.5 mm | In distribution |
| 01-03 | In distribution | |
| 01-3314 | Width 9.5 mm | In distribution |
| 01-9080-18T | Guidewire Diameter 1.4 mm | In distribution |
| 01-3014 | Height 14 mm | In distribution |
| 01-P1 | In distribution | |
| O-2700 | In distribution | |
| 01-04-3 | In distribution | |
| 01-06-1 | In distribution | |
| 01-05 | In distribution | |
| 01-B2 | In distribution | |
| 01-T2 | In distribution | |
| O-3000 | In distribution | |
| 01-3009 | Width 9.5 mm | In distribution |
| 01-00-2 | In distribution | |
| 01-14-1 | In distribution | |
| 01-C1 | In distribution | |
| 01-2001 | In distribution | |
| 01-14-5 | In distribution | |
| 01-3013 | Width 9.5 mm | In distribution |
| 01-2710 | Height 9.5 mm | In distribution |
Same 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
| Clearance | Decision date |
|---|---|
| K173947 | 2018-07-25 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Advanced Research Medical | 510(k) number | 2023-03-14 | Class II | Device Design | Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery. | 1150 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.
| 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.