Aptus A-5800.45/1
Active
510(k)
Valid until
No expiry
FDA recalls
2 ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07630008427214 | Date24 Oct 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK091479 | Date13 Jul 2009 | StatusActive |
Recalls
-
- Ongoing Z-1550-2026
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
-
- Ongoing Z-1821-2024
Screw is 16mm long instead of 22mm long.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aptus
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Model / Ref / Catalog
- A-5800.45/1
- Primary DI / UDI-DI
- 07630008427214
- 510(k) Number
- FDA product code
- HWC
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, non-sterile
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from Medartis Inc.
Properties
Other properties (11)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Over-the-counter: No
- Convenience kit: No
- Combination product: No
- HCT/P: No
- Premarket exempt: No
- Serial number: No
- Expiration date: No
- Manufacturing date: No