The following data is part of a premarket notification filed by Tornier with the FDA for Hls Uni Evolution Prosthesis.
Device ID | K022211 |
510k Number | K022211 |
Device Name: | HLS UNI EVOLUTION PROSTHESIS |
Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, 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 | HSX |
CFR Regulation Number | 888.3520 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-07-08 |
Decision Date | 2003-05-22 |
Summary: | summary |