The following data is part of a premarket notification filed by Osteonics Corp. with the FDA for Osteo Dynatroc Proximal Femoral Nail.
Device ID | K983339 |
510k Number | K983339 |
Device Name: | OSTEO DYNATROC PROXIMAL FEMORAL NAIL |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
Contact | Kate Sutton |
Correspondent | Kate Sutton OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-09-23 |
Decision Date | 1998-10-27 |
Summary: | summary |