Nancy Nail 8006-10-100
Nancy Nail 8006-10-100 (800610100) is a Class II device made by Biomet Orthopedics, Inc., cleared under FDA 510(k) K032687 on 6 Oct 2003 (1 earlier submission) and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00887868032844), 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 | GUDID listing | Number00887868032844 | Date24 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK032687 | Date6 Oct 2003 | StatusActive |
Official records
- AccessGUDID record 00887868032844
- FDA 510(k) database K032687
- FDA 510(k) database K960642
Across registries
- FDA 510(k) K032687 decided 6 Oct 2003 Active
- FDA GUDID UDI-DI 00887868032844 listed 24 Oct 2015 Listed
Timeline
- Cleared FDA 510(k) K960642
- Cleared FDA 510(k) K032687
- Listed FDA GUDID 00887868032844
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Nancy Nail
- Generic name
- Orthopaedic bone pin, non-bioabsorbable
- Model / Ref / Catalog
- 8006-10-100, 800610100
- Primary DI / UDI-DI
- 00887868032844
- FDA product code
- HTY
- GMDN term
- Orthopaedic bone pin, non-bioabsorbable
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
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