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 |