Clearance Summary
AOS INTERSTITIAL TEMPLATES, NEEDLES & ACCESSORIES received FDA 510(k) clearance under submission number K062823, sponsored by Alpha-Omega Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2007-05-29.
- Submission: K062823
- Applicant / Sponsor: Alpha-Omega Services, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5700
- Decision date: 2007-05-29
Classification & Regulation
This clearance is catalogued under FDA product code JAQ and 21 CFR 892.5700, within the Radiology review panel as a Class II device.