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 |