510(k) K081853
K081853 is an FDA 510(k) premarket notification submitted by Apollo Endosurgery, Inc. for the device "OVERSTITCH ENDOSCOPIC SUTURE SYSTEM". The FDA issued a decision of Substantially Equivalent on August 18, 2008. The device falls under product code OCW (Endoscopic Tissue Approximation Device), a Class II device regulated under 21 CFR 876.1500. Apollo Endosurgery, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 18, 2008
- Date Received
- June 30, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscopic Tissue Approximation Device
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
To aid in endoscopically placing sutures, staples, clips, and other fastening tools through tissue.