Clearance Summary
MEDI-PLINTH received FDA 510(k) clearance under submission number K924905, sponsored by Medi-Man Rehabilitation Products, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1993-02-16.
- Submission: K924905
- Applicant / Sponsor: Medi-Man Rehabilitation Products, Inc.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3760
- Decision date: 1993-02-16
Classification & Regulation
This clearance is catalogued under FDA product code INQ and 21 CFR 890.3760, within the Physical Medicine review panel as a Class I device.