Itotal® PS Ipoly® Insert Kit
3 catalogue numbers from RPS010200001, listed by ConforMIS, Inc., United States, under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer. 21 manufacturers in China are registered for this product code.
21manufacturers in China registered for this device type
3catalogue numbers in this listing
40510(k) clearances naming this product code
19recalls on this code
Who Else Makes It
Concentrated in Jiangsu (10), Shanghai (4), Beijing (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| MicroPort Orthopedics Global Supply Center Limited | Shanghai | Shanghai | Contract manufacturer | 82 |
| Zhejiang Biomet Medical Products Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 74 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Canwell Medical Co., Ltd. | Jinhua | Zhejiang | Contract manufacturer | 42 |
| Suzhou Elite Precision Machinery Co., Ltd. | Kunshan | Jiangsu | Contract manufacturer | 35 |
| Guangzhou Aquila Precise Tools Limited | Guangzhou | Guangdong | Contract manufacturer | 28 |
| B-ONE Medical (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 23 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Stryker (Suzhou) Medical Technology Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 10 |
| b-ONE Medical (Beijing) Co., Ltd. | Beijing | Beijing | Contract manufacturer | 7 |
| Changzhou Wastonortho Medical Appliance Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 5 |
Showing 12 of 21. All 21 manufacturers in China registered for Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Record
| Listed by | ConforMIS, Inc., United States |
|---|---|
| FDA product code | JWH |
| Device type | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3560 |
| Establishment | Remanufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K161668 |
| Record published | 2018-08-03 |
| Record revised | 2018-07-06 (version 3) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | expiry date, serial number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| RPS010200001 | 20 mm thick on the medial side, lateral side is patient specific | In distribution |
| RPS010140001 | 14mm thick on the medial side, lateral side is patient specific | In distribution |
| RPS010130001 | 13mm thick on the medial side, lateral side is patient specific | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Prophecy® | Microport Orthopedics Inc. | 4,423 |
| Exult Knee Replacement System | Corentec Co., Ltd. | 1,770 |
| Freedom | Maxx Orthopedics Inc. | 1,693 |
| Legion | Smith & Nephew, Inc. | 1,534 |
| MyKnee | Medacta International SA | 1,466 |
| Journey | Smith & Nephew, Inc. | 1,339 |
| Persona® | Zimmer, Inc. | 1,254 |
| DJO Surgical | Encore Medical, L.P. | 1,131 |
| U2 Total Knee System | United Orthopedic Corp. | 1,078 |
| CKS Plus | Shalby Advanced Technologies, Inc. | 1,024 |
| Lospa Modular Knee System | Corentec Co., Ltd. | 1,020 |
| Natural-Knee® | Zimmer, Inc. | 980 |
Showing 12 of 1,175. All products under Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K230846 | 2023-07-17 |
| K231233 | 2023-05-26 |
| K230844 | 2023-04-27 |
| K221404 | 2022-07-26 |
| K221059 | 2022-05-10 |
| K213389 | 2021-11-10 |
| K212411 | 2021-09-23 |
| K210809 | 2021-05-12 |
| K210191 | 2021-05-06 |
| K210252 | 2021-02-17 |
| K203447 | 2020-12-22 |
| K201023 | 2020-06-16 |
| K193105 | 2020-03-13 |
| K190562 | 2019-08-08 |
| K180906 | 2018-05-16 |
| K161668 | 2016-07-15 |
| K161366 | 2016-06-14 |
| K153721 | 2016-03-25 |
| K160025 | 2016-03-07 |
| K153217 | 2016-01-07 |
| K152704 | 2015-10-21 |
| K142404 | 2014-12-11 |
| K142161 | 2014-11-14 |
| K140833 | 2014-06-30 |
| K140423 | 2014-05-27 |
| K133560 | 2014-03-28 |
| K133256 | 2014-01-09 |
| K131467 | 2013-07-18 |
| K131019 | 2013-05-24 |
| K122870 | 2013-01-14 |
| K122991 | 2012-12-20 |
| K122033 | 2012-09-27 |
| K120316 | 2012-04-19 |
| K113378 | 2012-02-15 |
| K120068 | 2012-02-03 |
| K112780 | 2011-12-15 |
| K103117 | 2011-01-07 |
| K094050 | 2010-09-16 |
| K080936 | 2008-05-12 |
| K052687 | 2006-08-31 |
Recalls Naming This Product
10 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 |
|---|---|---|---|---|---|---|---|
| ConforMIS, Inc. | 510(k) number | 2020-02-03 | Class II | Mixed-up of materials/components | A limited number of tibial trays were labeled with an incorrect serial number and were delivered to the wrong customer accounts. | 2 | 2020-12-02 |
| ConforMIS, Inc. | 510(k) number | 2019-01-04 | Class II | Employee error | The labeling of the boxes and sterile pouches did not match the contents. | 2 | 2020-06-29 |
| ConforMIS, Inc. | 510(k) number | 2017-07-24 | Class II | Employee error | Implant kit mislabeled | 2 units | 2019-02-01 |
| ConforMIS, Inc. | 510(k) number | 2016-10-31 | Class II | Software Design Change | iView report displayed femoral cut measurements in the incorrect unit of measure (inches vs. mm). | 1 unit | 2017-01-11 |
| ConforMIS, Inc. | 510(k) number | 2016-01-28 | Class II | Packaging process control | Incorrect femoral component distributed | 1 unit | 2016-03-09 |
| ConforMIS, Inc. | 510(k) number | 2015-08-31 | Class II | Process design | May contain small amounts of ethylene glycol residue | 68 units | 2016-03-02 |
| ConforMIS, Inc. | 510(k) number | 2015-08-31 | Class II | Process design | May contain small amounts of ethylene glycol residue | 3 units | 2016-03-02 |
| ConforMIS, Inc. | 510(k) number | 2015-08-31 | Class II | Process design | May contain small amounts of ethylene glycol residue | 313 units | 2016-03-02 |
| ConforMIS, Inc. | 510(k) number | 2015-08-31 | Class II | Process design | May contain small amounts of ethylene glycol residue | 348 units | 2016-03-02 |
| ConforMIS, Inc. | 510(k) number | 2015-08-31 | Class II | Process design | May contain small amounts of ethylene glycol residue | 110 units | 2016-03-02 |
Recalls
9 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 |
|---|---|---|---|---|---|
| 2024-03-11 | Class II | Process design | Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot 540287. It was confirmed that Lot 540287 and Lot 508287 were swapped between the pouching and final pack. | 3 units | |
| 2022-02-22 | Class II | Nonconforming Material/Component | Incorrect tibial base plate implant packaged in kit | 1 unit | |
| 2020-07-20 | Class II | Packaging process control | Outer box labels for kit 0469247 correct, however the boxes contained the implants and jigs for 0468920 | 1 kit | 2021-06-21 |
| 2020-02-03 | Class II | Mixed-up of materials/components | A limited number of tibial trays were labeled with an incorrect serial number and were delivered to the wrong customer accounts. | 4 | 2020-12-02 |
| 2019-10-25 | Class II | Under Investigation by firm | Medial and lateral polyethylene inserts did not securely fit into the cobalt chrome tray implant. | 1 unit | 2020-05-20 |
| 2018-12-03 | Class II | Labeling mix-ups | The kits were prepared with incorrect patient ID labels and may contain incorrect components. | 2 | 2020-06-26 |
| 2016-10-18 | Class II | Labeling Change Control | Mislabeled: incorrect serial number on the F4 A/P cut guide iJig. | 2 units | 2016-12-07 |
| 2014-11-19 | Class II | Labeling mix-ups | Incorrect serial number of tibial inserts packaged in tray may result in inserts not fitting | 1 unit | 2015-10-08 |
| 2012-07-17 | Class II | Device Design | Addendum Labeling iTotal CR Surgical Technique with Detailed Instructions of Total CR Poly Insertion Technique | 1427 units | 2013-02-27 |
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.