Ace Nancy Nail
510(k) K032687
Ace Nancy Nail is a Class II device made by Depuy Orthopaedics, Inc., cleared under FDA 510(k) K032687 on 6 Oct 2003, 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 | NumberK032687 | Date6 Oct 2003 | StatusActive |
Official records
- FDA 510(k) database K032687
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- HTY
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3040
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K032687
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| NANCY NAIL 8006-10-100 | 800610100 / 8006-10-100 | 00887868032844 | — | On the market |
| NANCY NAIL AND ENDCAP KIT 8006-20-450 | 800620450 / 8006-20-450 | 00887868032851 | — | On the market |
| NANCY NAIL AND ENDCAP KIT 8006-25-450 | 800625450 / 8006-25-450 | 00887868032868 | — | On the market |
| NANCY NAIL AND ENDCAP KIT 8006-30-450 | 800630450 / 8006-30-450 | 00887868032875 | — | On the market |
| NANCY NAIL AND ENDCAP KIT 8006-35-450 | 800635450 / 8006-35-450 | 00887868032882 | — | On the market |
| NANCY NAIL AND ENDCAP KIT 8006-40-450 | 800640450 / 8006-40-450 | 00887868032899 | — | On the market |
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