The following data is part of a premarket notification filed by Tornier with the FDA for Hls Noetos System.
| Device ID | K013906 |
| 510k Number | K013906 |
| Device Name: | HLS NOETOS SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | TORNIER ZIRST-161, RUE LAVOISIER Montbonnot, FR 38330 |
| Contact | Mireille Lemery |
| Correspondent | Mireille Lemery TORNIER ZIRST-161, RUE LAVOISIER Montbonnot, FR 38330 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-11-26 |
| Decision Date | 2002-07-17 |
| Summary: | summary |