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 |