510(k) K152830
K152830 is an FDA 510(k) premarket notification submitted by Osstem Implant Co., Ltd. for the device "K3". The FDA issued a decision of Substantially Equivalent on Apr 20, 2017. The device falls under product code EIA (Unit, Operative Dental), a Class I device regulated under 21 CFR 872.6640. Osstem Implant Co., Ltd. has 67 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 20, 2017
- Date Received
- Sep 29, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Operative Dental
- Device Class
- Class I
- Regulation Number
- 872.6640
- Review Panel
- DE
- Submission Type
- 510(k)