510(k) K220994
K220994 is an FDA 510(k) premarket notification submitted by Ncs Lab Srl for the device "Shoulder PacemakerTM". The FDA issued a decision of Substantially Equivalent on Oct 14, 2022. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Ncs Lab Srl has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 14, 2022
- Date Received
- Apr 4, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type
- 510(k)