EJX — Anchor, Preformed Class I
FDA product code EJX covers "Anchor, Preformed", a Class I medical device regulated under 21 CFR 872.3130. Submissions are reviewed by the Dental panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- EJX
- Device Class
- Class I
- Regulation Number
- 872.3130
- Submission Type
- Review Panel
- DE
- Medical Specialty
- Dental
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K133088 | m and m dental studio | ZX-27 | January 2, 2015 |