The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for T2 Femoral Nail.
Device ID | K081152 |
510k Number | K081152 |
Device Name: | T2 FEMORAL NAIL |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | HOWMEDICA OSTEONICS CORP. 325 Corporate Drive Mahwah, NJ 07430 |
Contact | Danielle Hillman |
Correspondent | Danielle Hillman HOWMEDICA OSTEONICS CORP. 325 Corporate Drive Mahwah, NJ 07430 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-04-23 |
Decision Date | 2008-06-10 |
Summary: | summary |