The following data is part of a premarket notification filed by Tornier with the FDA for Rhs.
Device ID | K060438 |
510k Number | K060438 |
Device Name: | RHS |
Classification | Prosthesis, Elbow, Semi-constrained, Cemented |
Applicant | TORNIER 161 RUE LAVOISIER Montbonnot, Saint-ismier, FR 38334 |
Contact | Mireille Lemery |
Correspondent | Mireille Lemery TORNIER 161 RUE LAVOISIER Montbonnot, Saint-ismier, FR 38334 |
Product Code | JDB |
CFR Regulation Number | 888.3160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-02-21 |
Decision Date | 2006-04-18 |
Summary: | summary |