The following data is part of a premarket notification filed by Novabone Products, Llc with the FDA for Perioglas Putty-bioactive Bone Graft Gel.
| Device ID | K063596 |
| 510k Number | K063596 |
| Device Name: | PERIOGLAS PUTTY-BIOACTIVE BONE GRAFT GEL |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | NovaBone Products, LLC 13709 PROGRESS BLVD., #33 Alachua, FL 32615 |
| Contact | David M Gaisser |
| Correspondent | David M Gaisser NovaBone Products, LLC 13709 PROGRESS BLVD., #33 Alachua, FL 32615 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-12-04 |
| Decision Date | 2007-02-22 |
| Summary: | summary |