Clearance Summary
HALL STERNUM SAW received FDA 510(k) clearance under submission number K862474, sponsored by Hall Surgical, Division of Zimmer, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1986-07-17.
- Submission: K862474
- Applicant / Sponsor: Hall Surgical, Division of Zimmer, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4820
- Decision date: 1986-07-17
Classification & Regulation
This clearance is catalogued under FDA product code DWH and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.