Zeus-P
Zeus-P Interbody, 25L x 13W x 16H mm, 5.7 Degree Lordosis
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 | Spinal Elements, Inc., 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 | Specification developer, Complaint-file establishment, Manufacturer |
| Record published | 2021-01-09 |
| Record revised | 2022-11-08 (version 5) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Distribution end date | 2022-11-08 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 105-65-320909 | In distribution | |
| 105-65-260911 | In distribution | |
| 1-110926B | In distribution | |
| 65-300908 | In distribution | |
| 65-300911 | In distribution | |
| PL261314 | In distribution | |
| 105-65-320910 | In distribution | |
| 1-140922B | In distribution | |
| 1-140926B | In distribution | |
| 1-170926B | In distribution | |
| 1-160922B | In distribution | |
| 105-65-320911 | In distribution | |
| 65-220907 | In distribution | |
| PL261311 | In distribution | |
| 105-65-320915 | In distribution | |
| 65-220914 | In distribution | |
| 105-65-320913 | In distribution | |
| 1-070922B | In distribution | |
| PL261312 | In distribution | |
| 65-300909 | In distribution | |
| 105-65-260912 | In distribution | |
| 105-65-320914 | In distribution | |
| 1-170922B | In distribution | |
| 65-300915 | In distribution | |
| 1-150926B | In distribution | |
| 1-120926B | In distribution | |
| 105-65-220913 | In distribution | |
| 65-220917 | In distribution | |
| 1-180922B | In distribution | |
| PL261310 | In distribution | |
| 65-260917 | In distribution | |
| 65-300916 | In distribution | |
| 65-260915 | In distribution | |
| 65-320918 | In distribution | |
| 1-130922B | In distribution | |
| 65-260911 | In distribution | |
| 1-120922B | In distribution | |
| 65-300918 | In distribution | |
| 1-100922B | In distribution | |
| 105-65-260914 | In distribution | |
| 65-220918 | In distribution | |
| 65-300912 | In distribution | |
| 105-65-320912 | In distribution | |
| 1-150922B | In distribution | |
| 65-220908 | In distribution | |
| 105-65-220912 | In distribution | |
| 65-260913 | In distribution | |
| 65-300907 | In distribution | |
| 105-65-220909 | In distribution | |
| 65-320907 | In distribution | |
| 65-320917 | In distribution | |
| 65-260918 | In distribution | |
| 1-180926B | In distribution | |
| 105-65-260907 | In distribution | |
| 65-300914 | In distribution | |
| 1-070926B | In distribution | |
| 1-110922B | In distribution | |
| PL261309 | In distribution | |
| 65-260916 | In distribution | |
| 65-260908 | In distribution | |
| 1-090922B | In distribution | |
| PL261313 | In distribution | |
| 1-130926B | In distribution | |
| 65-220916 | In distribution | |
| 1-080926B | In distribution | |
| 105-65-260910 | In distribution | |
| 65-260909 | In distribution | |
| 1-080922B | In distribution | |
| 1-100926B | In distribution | |
| PL261315 | In distribution | |
| 105-65-220915 | In distribution | |
| 1-090926B | In distribution | |
| 65-300910 | In distribution | |
| 65-300917 | In distribution | |
| 105-65-320908 | In distribution | |
| PL261308 | In distribution | |
| 105-65-220910 | In distribution | |
| 1-160926B | In distribution | |
| 65-300913 | In distribution | |
| PH251311 | Withdrawn | |
| 105-65-220914 | Withdrawn | |
| PL251314 | Withdrawn | |
| 105-65-300915 | Withdrawn | |
| 1001111P | Withdrawn | |
| 105-65-320917 | Withdrawn | |
| 1001108BC | Withdrawn | |
| 1001109BC | Withdrawn | |
| PL251311 | Withdrawn | |
| 1001112BC | Withdrawn | |
| 1001116P | Withdrawn | |
| 105-65-260915 | Withdrawn | |
| 105-65-300917 | Withdrawn | |
| 105-65-220908 | Withdrawn | |
| 65-260910 | Withdrawn | |
| 105-65-300908 | Withdrawn | |
| PL251315 | Withdrawn | |
| 105-65-260918 | Withdrawn | |
| 65-260907 | Withdrawn | |
| PL251309 | Withdrawn | |
| 105-65-260917 | Withdrawn | |
| 65-320910 | Withdrawn | |
| 105-65-300912 | Withdrawn | |
| 65-320913 | Withdrawn | |
| 1001114P | Withdrawn | |
| 65-220912 | Withdrawn | |
| 65-260912 | Withdrawn | |
| 1001114BC | Withdrawn | |
| 105-65-320918 | Withdrawn | |
| 1001110BC | Withdrawn | |
| 105-65-300916 | Withdrawn | |
| 65-320915 | Withdrawn | |
| 1001111BC | Withdrawn | |
| 105-65-220917 | Withdrawn | |
| 65-220911 | Withdrawn | |
| PL251308 | Withdrawn | |
| PH251308 | Withdrawn | |
| 1001115P | Withdrawn | |
| 105-65-300914 | Withdrawn | |
| 65-320916 | Withdrawn | |
| 65-320908 | Withdrawn | |
| PH251314 | Withdrawn | |
| 65-320912 | Withdrawn | |
| 105-65-220907 | Withdrawn | |
| 105-65-300918 | Withdrawn | |
| 65-320909 | Withdrawn | |
| 1001113P | Withdrawn | |
| 105-65-320907 | Withdrawn | |
| 105-65-260916 | Withdrawn | |
| 1001108P | Withdrawn | |
| PH251312 | Withdrawn | |
| 105-65-260909 | Withdrawn | |
| PL251310 | Withdrawn | |
| 65-320914 | Withdrawn | |
| PH251315 | Withdrawn | |
| PH251310 | Withdrawn | |
| 105-65-260908 | Withdrawn | |
| 65-320911 | Withdrawn | |
| 1001113BC | Withdrawn | |
| PL251313 | Withdrawn | |
| 105-65-300911 | Withdrawn | |
| 1001115BC | Withdrawn | |
| 105-65-220918 | Withdrawn | |
| 65-220910 | Withdrawn | |
| 65-220909 | Withdrawn | |
| 105-65-300907 | Withdrawn | |
| PL251316 | Withdrawn | |
| 105-65-220916 | Withdrawn | |
| 1001112P | Withdrawn | |
| 105-65-300910 | Withdrawn | |
| 105-65-300909 | Withdrawn | |
| 105-65-300913 | Withdrawn | |
| PL251312 | Withdrawn | |
| 105-65-320916 | Withdrawn | |
| 1001110P | Withdrawn | |
| PH251316 | Withdrawn | |
| 1001109P | Withdrawn | |
| 65-220915 | Withdrawn | |
| 105-65-220911 | Withdrawn | |
| 105-65-260913 | Withdrawn | |
| 1001107P | Withdrawn | |
| PH251309 | Withdrawn | |
| 65-220913 | Withdrawn | |
| PH251313 | Withdrawn |
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 |
|---|---|
| K260506 | 2026-05-15 |
| K250773 | 2026-02-04 |
| K234150 | 2024-03-27 |
| K231252 | 2023-06-30 |
| K210044 | 2021-06-30 |
| K203254 | 2021-03-26 |
| K202298 | 2020-12-22 |
| K182584 | 2018-12-10 |
| K181837 | 2018-11-02 |
| K170235 | 2017-11-29 |
| K152011 | 2016-06-09 |
| K150061 | 2015-05-19 |
| K122967 | 2013-02-21 |
| K110632 | 2012-05-23 |
| K081968 | 2008-08-05 |
| K073348 | 2007-12-26 |
| K071724 | 2007-11-09 |
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2018-04-16 | Class II | Labeling mix-ups | Omega LIF interbody implants labeled as having 11 degrees of lordosis was assembled using components manufactured with 4 degrees of lordosis. | 19 units | |
| 2014-12-18 | Class II | Labeling False and Misleading | Spinal Elements is recalling the Ti-Bond related brochures that includes LT-10000 and MP-14000 (all revisions) the content regarding the Ti-Bond coating within the literature is unsubstantiated in context and/or misleading for the coating’s | 1200 units | 2015-03-10 |
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.