The following data is part of a premarket notification filed by Electro-biology, Inc. with the FDA for Modification To Ebi Spinelink System.
| Device ID | K982908 |
| 510k Number | K982908 |
| Device Name: | MODIFICATION TO EBI SPINELINK SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | ELECTRO-BIOLOGY, INC. 6 UPPER POND RD. P.O. BOX 345 Parsippany, NJ 07054 |
| Contact | Jonas Wilf |
| Correspondent | Jonas Wilf ELECTRO-BIOLOGY, INC. 6 UPPER POND RD. P.O. BOX 345 Parsippany, NJ 07054 |
| Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1998-08-18 |
| Decision Date | 1998-08-28 |
| Summary: | summary |