510(k) K223326
K223326 is an FDA 510(k) premarket notification submitted by Restor3D for the device "Axiom PSR System". The FDA issued a decision of Substantially Equivalent on March 30, 2023. The device falls under product code OYK (Ankle Arthroplasty Implantation System), a Class II device regulated under 21 CFR 888.3110. Restor3D has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 30, 2023
- Date Received
- October 31, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ankle Arthroplasty Implantation System
- Device Class
- Class II
- Regulation Number
- 888.3110
- Review Panel
- OR
- Submission Type
Intended to be used to assist in the implantation of a specific ankle arthroplasty device. Indicated to include guiding alignment, making or establishing cuts, and sizing.