The following data is part of a premarket notification filed by Degen Medical with the FDA for Impulse Am Interbody Fusion System.
| Device ID | K210090 |
| 510k Number | K210090 |
| Device Name: | Impulse AM Interbody Fusion System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | DeGen Medical 1321-C North Cashua Drive Florence, SC 29501 |
| Contact | Craig Black |
| Correspondent | Linda Braddon Secure BioMed Evaluations 7828 Hickory Flat Highway Suite 120 Woodstock, GA 30188 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-01-13 |
| Decision Date | 2021-08-30 |
| Summary: | summary |