The following data is part of a premarket notification filed by Orthomet, Inc. with the FDA for Axiom Total Knee System And Plus Total Knee System.
| Device ID | K922734 |
| 510k Number | K922734 |
| Device Name: | AXIOM TOTAL KNEE SYSTEM AND PLUS TOTAL KNEE SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | ORTHOMET, INC. 6301 CECILIA CIRCLE Minneapolis, MN 55439 -2713 |
| Contact | David Cannistraci |
| Correspondent | David Cannistraci ORTHOMET, INC. 6301 CECILIA CIRCLE Minneapolis, MN 55439 -2713 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-06-08 |
| Decision Date | 1992-09-10 |