The following data is part of a premarket notification filed by Biodynamic Technologies, Inc. with the FDA for Ez-fix Small Cannulated Screw System.
Device ID | K962987 |
510k Number | K962987 |
Device Name: | EZ-FIX SMALL CANNULATED SCREW SYSTEM |
Classification | Screw, Fixation, Bone |
Applicant | BIODYNAMIC TECHNOLOGIES, INC. 1425 EAST NEWPORT CENTER DR. Deerfield Beach, FL 33442 |
Contact | Danny Hodgeman |
Correspondent | Danny Hodgeman BIODYNAMIC TECHNOLOGIES, INC. 1425 EAST NEWPORT CENTER DR. Deerfield Beach, FL 33442 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-08-01 |
Decision Date | 1996-11-04 |