The following data is part of a premarket notification filed by Conformis, Inc. with the FDA for Conformis Itotal Posterior Stabilized Knee Replacement System.
| Device ID | K153217 |
| 510k Number | K153217 |
| Device Name: | ConforMIS ITotal Posterior Stabilized Knee Replacement System |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | ConforMIS, Inc. 28 Crosby Dr. Bedford, MA 01730 |
| Contact | Amita Shah |
| Correspondent | Amita Shah ConforMIS, Inc. 28 Crosby Dr. Bedford, MA 01730 |
| Product Code | JWH |
| Subsequent Product Code | OIY |
| Subsequent Product Code | OOG |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-11-05 |
| Decision Date | 2016-01-07 |
| Summary: | summary |