510(k) K955697 ยท DZE Implant, Endosseous, Root-Form
ABUTMENT RETRIEVAL KIT
| Applicant | Nobelpharma USA, Inc., Westmont IL, US |
| Decision | Substantially Equivalent, Jan 30, 1996 |
| Received | Dec 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955697
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 19, 2020 | Nobel Biocare Usa Llc Abutment Screw Retrieval Kit - Product Usage: The kit itself does not have a specific intended Use, but included devices have specific intended use as shown above. Terminated |
DZE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.