510(k) K182650
K182650 is an FDA 510(k) premarket notification submitted by Truemed Group, LLC for the device "Arzzt Distal Radius and Ulna System". The FDA issued a decision of Substantially Equivalent on Jun 10, 2019. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Truemed Group, LLC has 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 10, 2019
- Date Received
- Sep 24, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plate, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
- 510(k)