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 |