Stryker Constavac
510(k) K823284
Stryker Constavac is a Class I device made by Stryker Corp., cleared under FDA 510(k) K823284 on 14 Jan 1983, 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 | NumberK823284 | Date14 Jan 1983 | StatusActive |
Official records
- FDA 510(k) database K823284
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GCY
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4680
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
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