510(k) K050669
K050669 is an FDA 510(k) premarket notification submitted by Jeil Medical Corporation for the device "JEIL BONE FIXATION SYSTEM". The FDA issued a decision of Substantially Equivalent on May 26, 2005. 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
- May 26, 2005
- Date Received
- Mar 15, 2005
- 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)