The following data is part of a premarket notification filed by Consensus Orthopedics, Inc with the FDA for Consensus Knee System.
| Device ID | K102927 |
| 510k Number | K102927 |
| Device Name: | CONSENSUS KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uncemented, Porous, Coated, Polymer/metal/polymer |
| Applicant | Consensus Orthopedics, Inc 1115 WINFIELD WAY SUITE 100 El Dorado Hills, CA 95762 -9623 |
| Contact | Matthew Hull |
| Correspondent | Matthew Hull Consensus Orthopedics, Inc 1115 WINFIELD WAY SUITE 100 El Dorado Hills, CA 95762 -9623 |
| Product Code | MBH |
| CFR Regulation Number | 888.3565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-04 |
| Decision Date | 2011-01-26 |
| Summary: | summary |