The following data is part of a premarket notification filed by Zuga Medical, Inc. with the FDA for Zuga Dental Implant System.
| Device ID | K122664 |
| 510k Number | K122664 |
| Device Name: | ZUGA DENTAL IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | ZUGA MEDICAL, INC. P.O. BOX 566 Chesterland, OH 44026 -2141 |
| Contact | Karen E Warden, Phd |
| Correspondent | Karen E Warden, Phd ZUGA MEDICAL, INC. P.O. BOX 566 Chesterland, OH 44026 -2141 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-31 |
| Decision Date | 2013-04-30 |
| Summary: | summary |