Instinct™ Java® System 046W0AN35545
Instinct™ Java® System 046W0AN35545 is a Class II device made by Zimmer Spine, Inc., listed in FDA GUDID since 2 Oct 2015 (UDI-DI 00889024340718), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00889024340718 | Date2 Oct 2015 | StatusListed |
Official records
- AccessGUDID record 00889024340718
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Instinct™ Java® System
- Generic name
- Bone-screw internal spinal fixation system, non-sterile
- Model / reference
- 046W0AN35545
- Primary DI / UDI-DI
- 00889024340718
- FDA product code
- MNH, MNI, NKB
- GMDN term
- Bone-screw internal spinal fixation system, non-sterile
- Device class
- Class II
- Regulation number
- 888.3070
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 45 Millimeter
Similar devices
Other devices filed under FDA product code MNH (Orthosis, spondylolisthesis spinal fixation).
- Erisma™-LP 18455524 by Clariance, Inc.
- SHIRAZ-JAVA SPINAL FIXATION SYSTEM by Spine Next SA
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- MOSS 179710200 by Depuy Spine, Inc.
- AMSET R-F SYSTEM by Advanced Spine Technology, Inc.
- Erisma™-LP 18015540 by Clariance, Inc.
- CD HORIZON® Spinal System G154213555 by MEDTRONIC SOFAMOR DANEK, INC.
- Zavation Spinal System by ZAVATION
- ACROMED PEDICLE SCREW by Acromed Corp.