510(k) K231213
K231213 is an FDA 510(k) premarket notification submitted by Hankil Tech Medical Co., Ltd. for the device "HKT Anatomical Locking Trauma System". The FDA issued a decision of Substantially Equivalent on Jan 19, 2024. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Hankil Tech Medical Co., Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 19, 2024
- Date Received
- Apr 28, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plate, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type