ShurFit Acif 2c
The ShurFit ACIF 2C cage supports fusion at one cervical disc level from C3 to C7 in skeletally mature patients with degenerative disc disease. It is implanted from the front of the neck…
The ShurFit ACIF 2C cage supports fusion at one cervical disc level from C3 to C7 in skeletally mature patients with degenerative disc disease. It is implanted from the front of the neck using autograft bone and must be used with supplemental fixation. Patients should first have at least six weeks of nonoperative treatment.
The cage provides mechanical support at the treated level until biological fusion occurs. Its body is made of PEEK Optima LT1. The endplate coating combines a commercially pure titanium base layer with a hydroxyapatite layer over it.
Listed Item
CpTi + HA Coated ACIF Wide Cage Peek 05 degree x 11mm
Coated Implant Configuration
The coated cage is supplied sterile. The ShurFit family offers different widths, heights and lengths to accommodate patient anatomy and graft material. Degenerative disc disease means discogenic pain with degeneration confirmed by history and radiographic studies.
Who Else Makes It
Concentrated in Shanghai (2), Shandong (2), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Zibo Dante Co., Ltd. | Zibo | Shandong | Contract manufacturer | 17 |
| Zhisu Health Tech Jiaxing Co., Ltd. | Tongxiang | Zhejiang | Contract manufacturer | 4 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
| Zhejiang Decans Medical Devices Co., Ltd. | Jiaxing | Zhejiang | Manufacturer | 10 |
| Shanghai Sanyou Medical Co., Ltd. | Shanghai | Shanghai | Manufacturer | 6 |
Record
| Listed by | Precision Spine, Inc., United States |
|---|---|
| FDA product code | ODP |
| Device type | Intervertebral Fusion Device With Bone Graft, Cervical |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3080 |
| Establishment | Manufacturer |
| 510(k) | K161809 |
| Record published | 2019-03-27 |
| Record revised | 2025-07-14 (version 4) |
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, serial number |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 62-SC-0102 | In distribution | |
| ACIF10-11P-2C | In distribution | |
| 62-SC-0101 | In distribution | |
| ACIF05-10P-2C | In distribution | |
| 45-05-08P-2C | In distribution | |
| 45-05-11P-2C | In distribution | |
| 62-BK-0101 | In distribution | |
| 45-05-05P-2C | In distribution | |
| 45-05-06P-2C | In distribution | |
| ACIF10-08P-2C | In distribution | |
| 45-10-11P-2C | In distribution | |
| 45-10-12P-2C | In distribution | |
| 62-BK-0103 | In distribution | |
| 45-10-07P-2C | In distribution | |
| ACIF10-06P-2C | In distribution | |
| ACIF05-11P-2C | In distribution | |
| ACIF05-09P-2C | In distribution | |
| ACIF10-10P-2C | In distribution | |
| ACIF10-05P-2C | In distribution | |
| ACIF10-09P-2C | In distribution | |
| 45-10-10P-2C | In distribution | |
| ACIF10-07P-2C | In distribution | |
| 62-BK-0601 | In distribution | |
| 62-BK-0102 | In distribution | |
| 45-10-08P-2C | In distribution | |
| ACIF05-08P-2C | In distribution | |
| ACIF05-07P-2C | In distribution | |
| 45-05-09P-2C | In distribution | |
| ACIF05-06P-2C | In distribution | |
| 45-10-06P-2C | In distribution | |
| 45-05-07P-2C | In distribution | |
| 62-PC-0003 | In distribution | |
| ACIF10-12P-2C | In distribution | |
| 45-05-12P-2C | In distribution | |
| 45-05-10P-2C | In distribution | |
| ACIFXX-XXP-2C-CC | In distribution | |
| 45-10-05P-2C | In distribution | |
| 62-SC-0103 | In distribution | |
| ACIF05-12P-2C | In distribution | |
| 45-10-09P-2C | In distribution | |
| ACIF05-05P-2C | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Latitude-C AM™ Cervical Interbody Fusion System | Degen Medical | 1,529 |
| IdentiTi | Alphatec Spine, Inc. | 1,390 |
| Zavation | Zavation | 1,357 |
| IVA Cage Ti | Diomedical Co., Ltd. | 1,202 |
| Latitude-C Cervical Interbody Spacer System | Degen Medical | 1,185 |
| Peridot Anterior Cervical Intervertebral Body Fusion System | Gbs Commonwealth Co., Ltd. | 1,056 |
| Aleutian® Interbody Systems | VB Spine LLC | 1,017 |
| Valeo Spacer System | Sintx Technologies Inc. | 918 |
| Cascadia™ Interbody System | VB Spine LLC | 823 |
| CoRoent | Nuvasive, Inc. | 815 |
| Tyber Medical | Tyber Medical | 740 |
| Matisse Anterior Cervical Interbody Fusion Cage System | CTL Medical Corporation | 577 |
Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K250769 | 2025-11-24 |
| K161809 | 2016-12-06 |
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.