CHS
Intertan Compression Screw 30MM
3manufacturers in China registered for this device type
1catalogue number
12510(k) clearances naming this product code
8recalls on this code
Who Else Makes It
Concentrated in Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Zimmer (Shanghai) Medical International Trading Co., Ltd. | Shanghai | Shanghai | Exporter | 106 |
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
Record
| Listed by | Smith & Nephew, Inc., United States |
|---|---|
| FDA product code | JDS |
| Device type | Nail, Fixation, Bone |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3030 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K040212 |
| Record published | 2015-08-25 |
| Record revised | 2025-02-06 (version 8) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 71672030 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Autobahn | Globus Medical, Inc. | 1,102 |
| Trigen | Smith & Nephew, Inc. | 1,062 |
| Nail, Fixation, Bone | Synthes Gmbh | 296 |
| Nail, Fixation, Bone | Synthes (U.S.A.) LP | 237 |
| Intertan MAX | Smith & Nephew, Inc. | 235 |
| EXPert Nail | Synthes Gmbh | 225 |
| Trigen MAX | Smith & Nephew, Inc. | 172 |
| Ajax Nail | Auxein medical Private limited | 168 |
| GPC | GPC Medical Limited | 155 |
| 130° Ga-mma Nail | Auxein medical Private limited | 90 |
| Ender Nail | Smith & Nephew, Inc. | 82 |
| Centronail Titanium Humeral Nailing System | Orthofix SRL | 79 |
Showing 12 of 112. All products under Nail, Fixation, Bone
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K243608 | 2025-06-12 |
| K240061 | 2024-09-20 |
| K241804 | 2024-08-22 |
| K230761 | 2023-06-14 |
| K123948 | 2013-03-14 |
| K061783 | 2006-08-10 |
| K061019 | 2006-06-06 |
| K051557 | 2005-06-30 |
| K050938 | 2005-05-04 |
| K040212 | 2004-02-20 |
| K983942 | 1998-12-04 |
| K981529 | 1998-07-09 |
Recalls Naming This Product
6 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Smith & Nephew Orthopaedics AG | 510(k) number | 2022-04-22 | Class II | Under Investigation by firm | Right nails were anodized, marked, and labelled as left nails and vice versa | 17 units | |
| Smith & Nephew, Inc. | 510(k) number | 2020-11-02 | Class II | Packaging process control | Manufacturing packaging error. | 41 units | 2023-01-06 |
| Smith & Nephew, Inc. | 510(k) number | 2017-10-24 | Class II | Employee error | A single lot of INTERTAN 10S 10 MM X 18 CM 130 D was manufactured with the screw inserted upside down. | 17 units | |
| Smith & Nephew, Inc. | 510(k) number | 2014-07-02 | Class II | Under Investigation by firm | There was an error in manufacturing which resulted in the proximal lag screw hole being positioned incorrectly in several batches of TRIGEN(R); INTERTAN(TM); NAILS. | 601 units | 2019-08-20 |
| Smith & Nephew, Inc. | 510(k) number | 2014-04-04 | Class II | Process control | A manufacturing error resulted in the set screw being inserted too deep in the affected nails. | 1,253 units total | 2017-07-01 |
| Smith & Nephew, Inc. | 510(k) number | 2014-04-04 | Class II | Process control | A manufacturing error resulted in the set screw being inserted too deep in the affected nails. | 1,253 units total | 2017-07-01 |
Recalls
3 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 |
|---|---|---|---|---|---|
| 2020-06-24 | Class II | Reprocessing Controls | A manufacturing error which resulted in the re-sterilization of the ultra-high-molecular-weight polyethylene (UHMWPE) sleeve. | 12 units | 2021-04-28 |
| 2013-02-07 | Class II | Labeling mix-ups | 75 mm screws were packaged and labeled using an 80 mm screw outer box and label, while 80 mm screws were packaged and labeled using a 75 mm screw outer box and label. | 90 units | 2016-01-11 |
| 2013-02-07 | Class II | Labeling mix-ups | 75 mm screws were packaged and labeled using an 80 mm screw outer box and label, while 80 mm screws were packaged and labeled using a 75 mm screw outer box and label. | 69 units | 2016-01-11 |
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.