510(k) K220511
K220511 is an FDA 510(k) premarket notification submitted by Medline Industries, LP for the device "Medline UNITE IM Fibula Implant". The FDA issued a decision of Substantially Equivalent on Mar 22, 2022. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Medline Industries, LP has 268 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 22, 2022
- Date Received
- Feb 22, 2022
- Clearance Type
- Special
- 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)