The following data is part of a premarket notification filed by Depuy Acromed with the FDA for Modification To Symphony Graft Delivery System.
| Device ID | K010320 |
| 510k Number | K010320 |
| Device Name: | MODIFICATION TO SYMPHONY GRAFT DELIVERY SYSTEM |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
| Contact | Karen F Jurczak |
| Correspondent | Karen F Jurczak DEPUY ACROMED 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-02-02 |
| Decision Date | 2001-03-01 |