510(k) K220319
K220319 is an FDA 510(k) premarket notification submitted by Stryker GmbH for the device "Asnis III Cannulated Screw System, Asnis PRO Cannulated Screw System". The FDA issued a decision of Substantially Equivalent on Jun 10, 2022. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Stryker GmbH has 270 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 10, 2022
- Date Received
- Feb 3, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type
- 510(k)