The following data is part of a premarket notification filed by Blue Sky Bio, Llc with the FDA for Modification To Blue Sky Bio Dental Implant System.
| Device ID | K060957 |
| 510k Number | K060957 |
| Device Name: | MODIFICATION TO BLUE SKY BIO DENTAL IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | BLUE SKY BIO, LLC 888 E BELVIDERE RD. SUITE 212 Grayslake, IL 60030 |
| Contact | Michelle Vovolka |
| Correspondent | Michelle Vovolka BLUE SKY BIO, LLC 888 E BELVIDERE RD. SUITE 212 Grayslake, IL 60030 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-04-07 |
| Decision Date | 2006-05-05 |
| Summary: | summary |