510(k) K202151
K202151 is an FDA 510(k) premarket notification submitted by Techmah Medical, LLC for the device "Smart SPACE Shoulder System". The FDA issued a decision of Substantially Equivalent on Feb 3, 2021. The device falls under product code QHE (Shoulder Arthroplasty Implantation System), a Class II device regulated under 21 CFR 888.3660. Techmah Medical, LLC has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 3, 2021
- Date Received
- Aug 3, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Shoulder Arthroplasty Implantation System
- Device Class
- Class II
- Regulation Number
- 888.3660
- Review Panel
- OR
- Submission Type
- 510(k)
Intended to be used to assist in the implantation of a specific shoulder arthroplasty device or a set of specific shoulder arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components.