510(k) K011740
K011740 is an FDA 510(k) premarket notification submitted by Meddev Corp. for the device "CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)". The FDA issued a decision of Substantially Equivalent on July 2, 2001. The device falls under product code MML (Weights, Eyelid, External), a Class II device regulated under 21 CFR 886.5700. Meddev Corp. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 2, 2001
- Date Received
- June 5, 2001
- Clearance Type
- Special
- 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)