510(k) K150986
K150986 is an FDA 510(k) premarket notification submitted by Meddev Corporation for the device "Contour Eyelid Weight Implants, ThinProfile Eyelid Weight Implants". The FDA issued a decision of Substantially Equivalent on August 17, 2015. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 17, 2015
- Date Received
- April 14, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Weights, Eyelid, External
- Device Class
- Class II
- Regulation Number
- 886.5700
- Review Panel
- OP
- Submission Type
Gravity assisted treatment of lagophthalmos (incomplete eyelid closure)