510(k) K241995
K241995 is an FDA 510(k) premarket notification submitted by Footbridge Medical for the device "HyperFlex Bunion Correction System". The FDA issued a decision of Substantially Equivalent on November 26, 2024. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 26, 2024
- Date Received
- July 9, 2024
- 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