510(k) K173693
K173693 is an FDA 510(k) premarket notification submitted by Orthovestments, LLC for the device "Orbitum Bone Staple Implant, X and VI". The FDA issued a decision of Substantially Equivalent on Feb 23, 2018. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 23, 2018
- Date Received
- Dec 1, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
- 510(k)