Pass MIS
CANNULATED POLYAXIAL PEDICLE SCREW Ø 7.5mm x 60mm
13manufacturers in China registered for this device type
228catalogue numbers in this listing
10510(k) clearances naming this product code
1recall
Who Else Makes It
Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 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 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| APS Materials Suzhou | Suzhou | Jiangsu | Contract manufacturer | 18 |
| Zibo Dante Co., Ltd. | Zibo | Shandong | Contract manufacturer | 17 |
| Shanghai JPY ION-Tech Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 70 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Johnson & Johnson Medical (Depuy – Suzhou) Ltd. | Suzhou | Jiangsu | Manufacturer | 34 |
| Double Medical Technology Inc. | Xiamen | Fujian | Contract manufacturer | 14 |
| Suzhou Kangli Orthopaedics Instrument Co., Ltd. | Zhangjiagang | Jiangsu | Contract manufacturer | 11 |
| Changzhou Yonghua Medical Instruments Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 8 |
| Jiangsu Ideal Medical Science & Technology Co., Ltd. | Zhangjiagang | Jiangsu | Contract manufacturer | 7 |
Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spinal Pedicle Fixation
Record
| Listed by | Medicrea International, France |
|---|---|
| FDA product code | MNI |
| Device type | Orthosis, Spinal Pedicle Fixation |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3070 |
| Establishment | Specification developer, Manufacturer |
| Record published | 2015-10-23 |
| Record revised | 2025-07-02 (version 8) |
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 | 2023-08-04 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| B06020455 | In distribution | |
| B06020860 | In distribution | |
| B06017560 | Withdrawn | |
| B06037200S | Withdrawn | |
| B06033180S | Withdrawn | |
| B06037070 | Withdrawn | |
| B06015550 | Withdrawn | |
| B06031080 | Withdrawn | |
| B06033070S | Withdrawn | |
| B06032030S | Withdrawn | |
| B06031080S | Withdrawn | |
| B06031160S | Withdrawn | |
| B06033080S | Withdrawn | |
| B06017555 | Withdrawn | |
| B06033200 | Withdrawn | |
| B06047545 | Withdrawn | |
| B06015035 | Withdrawn | |
| B06031030 | Withdrawn | |
| B06033060 | Withdrawn | |
| B06015560 | Withdrawn | |
| B06031200S | Withdrawn | |
| B06035240 | Withdrawn | |
| B06031220 | Withdrawn | |
| B06015530 | Withdrawn | |
| B06031240S | Withdrawn | |
| B06046530 | Withdrawn | |
| B06032050S | Withdrawn | |
| B06034080 | Withdrawn | |
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| B06016530 | Withdrawn | |
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| B06015545 | Withdrawn | |
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| B06033120S | Withdrawn | |
| B06033160S | Withdrawn | |
| B06033260 | Withdrawn | |
| B06032070S | Withdrawn | |
| B06031200 | Withdrawn | |
| B06033240S | Withdrawn | |
| B06037100 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| CD Horizon® Spinal System | Medtronic Sofamor Danek, Inc. | 2,342 |
| Creo | Globus Medical, Inc. | 1,784 |
| ReLine | Nuvasive, Inc. | 1,718 |
| AnyPlus Spinal Fixation System | GS Medical Co., Ltd. | 1,525 |
| Apex Spine System | Spinecraft LLC | 1,114 |
| Revere | Globus Medical, Inc. | 1,051 |
| LnK Spinal Fixation System | L&K Biomed Co., Ltd. | 974 |
| LnK Basic Spinal Fixation System | L&K Biomed Co., Ltd. | 935 |
| Arsenal | Alphatec Spine, Inc. | 932 |
| Zavation | Zavation | 864 |
| Polaris™ 5.5 Spinal System | Biomet Spine | 809 |
| Apex-DL Spine System | Spinecraft LLC | 792 |
Showing 12 of 950. All products under Orthosis, Spinal Pedicle Fixation
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K150049 | 2015-02-10 |
| K140738 | 2014-11-04 |
| K112493 | 2011-11-21 |
| K100297 | 2010-03-04 |
| K083810 | 2009-07-31 |
| K083308 | 2008-12-10 |
| K082069 | 2008-10-03 |
| K080099 | 2008-04-09 |
| K070276 | 2007-09-21 |
| K062136 | 2006-10-06 |
Recalls
1 of these is 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 |
|---|---|---|---|---|
| 2023-07-12 | Class II | Under Investigation by firm | There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch. | 963 units |
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.