510(k) K142569
K142569 is an FDA 510(k) premarket notification submitted by Aptis Medical, LLC for the device "Aptis Medical Distal Radio Ulnar Joint Implant". The FDA issued a decision of Substantially Equivalent on April 3, 2015. The device falls under product code KXE (Prosthesis, Wrist, Hemi-, Ulnar), a Class II device regulated under 21 CFR 888.3810. Aptis Medical, LLC has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 3, 2015
- Date Received
- September 12, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Wrist, Hemi-, Ulnar
- Device Class
- Class II
- Regulation Number
- 888.3810
- Review Panel
- OR
- Submission Type