VERASENSE for Stryker Triathlon
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816818021584 | Date18 Nov 2020 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Arthroplasty force sensor
- Model / Ref / Catalog
- VERASENSE for Stryker Triathlon CR Size 7, SYK-TRCR07
- Primary DI / UDI-DI
- 00816818021584
- FDA Product Code
- ONN
- GMDN Term
- Arthroplasty force sensor
- Device Class
- Class II
- Regulation Number
- 882.4560
- GUDID distribution status
- Not in Commercial Distribution
Other devices from Orthosensor Inc
Properties
Other properties (7)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No