PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS— 510(k) K072572
Substantially EquivalentLifecore Biomedical, Inc.
FDA 510(k) clearance K072572 for PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS, Substantially Equivalent on 2007-10-05. Applicant: Lifecore Biomedical, Inc.. Device class: 2.
Clearance details
- Applicant
- Lifecore Biomedical, Inc.
- Product code
- Code NHA
- Device class
- Class 2
- Regulation
- 21 CFR 872.3630
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Chaska, MN, US
Recent devices under product code NHA
view allMore clearances from Lifecore Biomedical, Inc.
view all- K073032 — PRIMACONNEX SD ESTHETIC CONTOUR ZI ABUTMENTS
- K072241 — PRIMACONNEX CAD/CAM ABUTMENT SYSTEM
- K072768 — RESTORE, STAGE-1, RENOVA PRIMASOLO AND PRIMACONNEX DENTAL IMPLANTS
- K062876 — PRIMACONNEX CERAMIC ABUTMENTS
- K060530 — SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.
Adverse events under product code NHA
product code NHA- Injury
- 1,270
- Malfunction
- 2,860
- Total
- 4,130
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.