Table, Hand Surgi
510(k) K760456
Table, Hand Surgi is a Class I device made by Stryker Corp., cleared under FDA 510(k) K760456 on 2 Nov 1976, 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 | NumberK760456 | Date2 Nov 1976 | StatusActive |
Official records
- FDA 510(k) database K760456
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- FWZ
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4950
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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