The following data is part of a premarket notification filed by Tornier with the FDA for Hls Kneetec System.
| Device ID | K094013 |
| 510k Number | K094013 |
| Device Name: | HLS KNEETEC SYSTEM |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | TORNIER 161 RUE LAVOISIER Montbonnot, Saint-ismier, FR 38334 |
| Contact | Severine Bonneton |
| Correspondent | Severine Bonneton TORNIER 161 RUE LAVOISIER Montbonnot, Saint-ismier, FR 38334 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-12-29 |
| Decision Date | 2011-05-05 |
| Summary: | summary |