The following data is part of a premarket notification filed by Ebi, L.p. with the FDA for Modification To Ebi Efix Vision Fixation System.
| Device ID | K011711 |
| 510k Number | K011711 |
| Device Name: | MODIFICATION TO EBI EFIX VISION FIXATION SYSTEM |
| Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
| Applicant | EBI, L.P. 399 JEFFERSON ROAD Parsippany, NJ 07054 |
| Contact | Patricia Flood |
| Correspondent | Patricia Flood EBI, L.P. 399 JEFFERSON ROAD Parsippany, NJ 07054 |
| Product Code | KTT |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-06-04 |
| Decision Date | 2001-06-29 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00880304529854 | K011711 | 000 |
| 00887868090028 | K011711 | 000 |
| 00888480187745 | K011711 | 000 |
| 00888480187769 | K011711 | 000 |
| 00888480188049 | K011711 | 000 |
| 00888480188100 | K011711 | 000 |
| 00880304485174 | K011711 | 000 |
| 00880304486553 | K011711 | 000 |
| 00880304496361 | K011711 | 000 |
| 00887868090004 | K011711 | 000 |