INT — Plinth Class I
FDA product code INT covers "Plinth", a Class I medical device regulated under 21 CFR 890.3520. Submissions are reviewed by the Physical Medicine panel. At least 4 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- INT
- Device Class
- Class I
- Regulation Number
- 890.3520
- Submission Type
- Review Panel
- PM
- Medical Specialty
- Physical Medicine
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K770723 | chattanooga pharmacal | TABLE, TREATMENT, THERAPY, PHYSICAL | July 11, 1977 |
| K770636 | i e industries | TABLE, EXAM & MANUPULATION | April 15, 1977 |
| K770609 | will ross | TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT | April 8, 1977 |
| K770509 | will ross | TABLE, MASSAGE AND TREATMENT | April 5, 1977 |