LGG — Instrument, Cast Application/Removal, Manual Class I
FDA Device Classification
Classification Details
- Product Code
- LGG
- Device Class
- Class I
- Regulation Number
- 888.5980
- Submission Type
- Review Panel
- OR
- Medical Specialty
- Orthopedic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K870100 | orthopedic systems | PLASTER STAND | January 28, 1987 |
| K851786 | artiberia | 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF | July 9, 1985 |
| K834384 | buckman co | MODULAR EXTREMITY CASTING SUPPORT | January 30, 1984 |