Clearance Summary
TPG 1000 received FDA 510(k) clearance under submission number K831002, sponsored by Physical Diagnostics, 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 1983-06-24.
- Submission: K831002
- Applicant / Sponsor: Physical Diagnostics, Inc.
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class I
- Regulation citation: 21 CFR 888.5890
- Decision date: 1983-06-24
Classification & Regulation
This clearance is catalogued under FDA product code KQZ and 21 CFR 888.5890, within the Orthopedic review panel as a Class I device.