Clearance Summary
LUNDEEN SUBTALAR PEG IMPLANT received FDA 510(k) clearance under submission number K922292, sponsored by Sgarlato Laboratories, 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 1992-10-23.
- Submission: K922292
- Applicant / Sponsor: Sgarlato Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3040
- Decision date: 1992-10-23
Classification & Regulation
This clearance is catalogued under FDA product code MJW and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.