Mariner MCT MC2-003025
by SeaSpine Orthopedics Corporation
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10889981189433 | Date9 Jan 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173882 | Date6 Feb 2018 | StatusActive |
Recalls
-
- Ongoing Z-2762-2026
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Mariner MCT
- Generic name
- Orthopaedic inorganic implant inserter/extractor, reusable
- Model / Ref / Catalog
- MC2-003025
- Primary DI / UDI-DI
- 10889981189433
- 510(k) Number
- FDA product code
- NKB
- GMDN term
- Orthopaedic inorganic implant inserter/extractor, reusable
- Device class
- Class II
- Regulation number
- 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Other devices from SeaSpine Orthopedics Corporation
Properties
Other properties (12)
- Supplied sterile: No
- Single use: 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