Medyssy Lt Cage System
510(k) K121246
Medyssy Lt Cage System is a Class II device made by Medyssey Co., Ltd., cleared under FDA 510(k) K121246 on 15 Jun 2012, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK121246 | Date15 Jun 2012 | StatusActive |
Official records
- FDA 510(k) database K121246
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MAX
- FDA applicant
- Medyssey Co, Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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