The following data is part of a premarket notification filed by Biodynamic Technologies, Inc. with the FDA for Ez-6 Proximal Humeral Interamedullary Rod System.
Device ID | K962552 |
510k Number | K962552 |
Device Name: | EZ-6 PROXIMAL HUMERAL INTERAMEDULLARY ROD SYSTEM |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | BIODYNAMIC TECHNOLOGIES, INC. EAST NEWPORT CENTER DR. Deerfield Beach, FL 33442 |
Contact | Danny Hodgeman |
Correspondent | Danny Hodgeman BIODYNAMIC TECHNOLOGIES, INC. EAST NEWPORT CENTER DR. Deerfield Beach, FL 33442 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-01 |
Decision Date | 1996-09-25 |
Summary: | summary |