The following data is part of a premarket notification filed by Richards Medical Co., Inc. with the FDA for Tricon M Total Knee System.
| Device ID | K833200 |
| 510k Number | K833200 |
| Device Name: | TRICON M TOTAL KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patello/femorotibial, Semi-constrained, Uhmwpe, Pegged, Cemented, Polymer/metal/polymer |
| Applicant | RICHARDS MEDICAL CO., INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | MBV |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-19 |
| Decision Date | 1983-11-29 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00885556049815 | K833200 | 000 |
| 00885556049808 | K833200 | 000 |