The following data is part of a premarket notification filed by Dentsply Interntional with the FDA for Osteograf/n-300.
| Device ID | K071817 |
| 510k Number | K071817 |
| Device Name: | OSTEOGRAF/N-300 |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | DENTSPLY INTERNTIONAL 221 W. PHILADELPHIA ST. STE.60 SUSQUEHANNA COMMERCE CRT. WEST York, PA 17404 |
| Contact | Helen Lewis |
| Correspondent | Helen Lewis DENTSPLY INTERNTIONAL 221 W. PHILADELPHIA ST. STE.60 SUSQUEHANNA COMMERCE CRT. WEST York, PA 17404 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-07-03 |
| Decision Date | 2007-09-04 |
| Summary: | summary |