Clearance Summary
MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA received FDA 510(k) clearance under submission number K964350, sponsored by Intermedics Orthopedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1997-01-16.
- Submission: K964350
- Applicant / Sponsor: Intermedics Orthopedics
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3350
- Decision date: 1997-01-16
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.