510(k) K183162
K183162 is an FDA 510(k) premarket notification submitted by Biomet, Inc. for the device "Affixus Hip Fracture Nail". The FDA issued a decision of Substantially Equivalent on Dec 14, 2018. The device falls under product code HSB (Rod, Fixation, Intramedullary And Accessories), a Class II device regulated under 21 CFR 888.3020. Biomet, Inc. has 443 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 14, 2018
- Date Received
- Nov 15, 2018
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Rod, Fixation, Intramedullary And Accessories
- Device Class
- Class II
- Regulation Number
- 888.3020
- Review Panel
- OR
- Submission Type
- 510(k)