510(k) K193432
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 9, 2020
- Date Received
- December 10, 2019
- 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.