Olympia 2870GK48
by Wright Medical Technology, Inc.
Olympia 2870GK48 is a Class II device made by Wright Medical Technology, Inc., listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00840420188984), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00840420188984 | Date17 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00840420188984
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Olympia
- Generic name
- Shoulder glenoid fossa prosthesis trial
- Model / Ref / Catalog
- 2870GK48
- Primary DI / UDI-DI
- 00840420188984
- FDA product code
- KWS
- GMDN term
- Shoulder glenoid fossa prosthesis trial
- Device class
- Class II
- Regulation number
- 888.3660
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 48 Millimeter
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