510(k) K091679
K091679 is an FDA 510(k) premarket notification submitted by Jeil Medical Corporation for the device "LEFORTE SYSTEM BONE PLATE". The FDA issued a decision of Substantially Equivalent on Oct 2, 2009. The device falls under product code JEY (Plate, Bone), a Class II device regulated under 21 CFR 872.4760. Jeil Medical Corporation has 52 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 2, 2009
- Date Received
- Jun 9, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Plate, Bone
- Device Class
- Class II
- Regulation Number
- 872.4760
- Review Panel
- DE
- Submission Type
- 510(k)