510(k) K213199
K213199 is an FDA 510(k) premarket notification submitted by Stryker GmbH for the device "Asnis® III Cannulated Screw System and Asnis® PRO Cannulated Screw System". The FDA issued a decision of Substantially Equivalent on Jan 11, 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
- Jan 11, 2022
- Date Received
- Sep 29, 2021
- 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)