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 |