Clearance Summary
ALTOMEC ARTHROSCOPE received FDA 510(k) clearance under submission number K112548, sponsored by Altomec Endoscopy, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2012-08-15.
- Submission: K112548
- Applicant / Sponsor: Altomec Endoscopy, Inc.
- Clearance pathway: Abbreviated
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.1100
- Decision date: 2012-08-15
Classification & Regulation
This clearance is catalogued under FDA product code HRX and 21 CFR 888.1100, within the Orthopedic review panel as a Class II device.