Astra Tech, Inc. · Class II · Cleared Jul 5, 2012
| K-number | K120338 |
| Device name | ATLANTIS IN ZIRCONIA FOR DENTSPLY ANKYLOS IMPLANT, ATLANTIS LATER ABUTMENT IN ZIRCONIA |
| Applicant | Astra Tech, Inc. |
| Product code | NHA |
| Device class | Class II |
| Decision date | Jul 5, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 872.3630 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov