510(k) K172698
K172698 is an FDA 510(k) premarket notification submitted by Orthofix Srl for the device "G-Beam Fusion Beaming System". The FDA issued a decision of Substantially Equivalent on Feb 7, 2018. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Orthofix Srl has 97 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 7, 2018
- Date Received
- Sep 7, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type
- 510(k)