The following data is part of a premarket notification filed by Electro-biology, Inc. with the FDA for Ebi Spinelink Anterior Cervical Spinal System.
| Device ID | K991092 |
| 510k Number | K991092 |
| Device Name: | EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | ELECTRO-BIOLOGY, INC. 100 INTERPACE PKWY. Parsippany, NJ 07054 |
| Contact | Jonas Wilf |
| Correspondent | Jonas Wilf ELECTRO-BIOLOGY, INC. 100 INTERPACE PKWY. Parsippany, NJ 07054 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-04-01 |
| Decision Date | 1999-04-29 |
| Summary: | summary |