510(k) K871777
K871777 is an FDA 510(k) premarket notification submitted by Van-Tec, Inc. for the device "VAN-TEC REUSABLE HELICAL STONE BASKET". The FDA issued a decision of Substantially Equivalent on June 17, 1987. The device falls under product code FFL (Dislodger, Stone, Basket, Ureteral, Metal), a Class II device regulated under 21 CFR 876.4680. Van-Tec, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 1987
- Date Received
- May 6, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dislodger, Stone, Basket, Ureteral, Metal
- Device Class
- Class II
- Regulation Number
- 876.4680
- Review Panel
- GU
- Submission Type