Clearance Summary
PROBE received FDA 510(k) clearance under submission number K800729, sponsored by Stainless Mfg., 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 1980-04-08.
- Submission: K800729
- Applicant / Sponsor: Stainless Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.4540
- Decision date: 1980-04-08
Classification & Regulation
This clearance is catalogued under FDA product code HXB and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.