Clearance Summary
SL-PLUS AND SLR-PLUS received FDA 510(k) clearance under submission number K932481, sponsored by Encore Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1994-06-08.
- Submission: K932481
- Applicant / Sponsor: Encore Orthopedics, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3350
- Decision date: 1994-06-08
Classification & Regulation
This clearance is catalogued under FDA product code JDI and 21 CFR 888.3350, within the Orthopedic review panel as a Class II device.