The following data is part of a premarket notification filed by Electro-biology, Inc. with the FDA for Ebi X Fix Dynafix System (dfs).
Device ID | K953406 |
510k Number | K953406 |
Device Name: | EBI X FIX DYNAFIX SYSTEM (DFS) |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | ELECTRO-BIOLOGY, INC. COLOMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
Contact | Jonathan S Kahan |
Correspondent | Jonathan S Kahan ELECTRO-BIOLOGY, INC. COLOMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-07-20 |
Decision Date | 1995-10-31 |