6002-710-050
6002-710-050 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 26 Jul 2022 (UDI-DI 07613327551938), registry data as of 23 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 | Number07613327551938 | Date26 Jul 2022 | StatusListed |
Official records
- AccessGUDID record 07613327551938
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Optical surgical tracking system spatial marker, reusable
- Model / Ref / Catalog
- 6002-710-050
- Primary DI / UDI-DI
- 07613327551938
- FDA product code
- OLO
- GMDN term
- Optical surgical tracking system spatial marker, reusable
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code OLO (Orthopedic stereotaxic instrument).
- ORTHOPILOT NEXT GENERATION-UKA SOFTWARE, MODEL FS210 by Aesculap Implant Systems, Inc.
- Spineology Navigation Instruments by SPINEOLOGY INC.
- OMNIBotics NS-5014L by OMNIlife science, Inc.
- 9735283 by Medtronic Navigation Inc.
- 9735284 by Medtronic Navigation Inc.
- TMINI™ Miniature Robotic System by Think Surgical Inc.
- 7D Registration Frame, 7D Flex Iliac Pin Connector, 7D Pin Guide Block, 7D 3.2 mm Steinmann Pin, 7D Iliac Crest Pin Chuck & Key by 7D Surgical, Inc.
- TMINI Miniature Robotic System (TMINI 1.1) by Think Surgical Inc.
- iASSIST Knee System by Orthosoft Inc. (d/b/a) Zimmer CAS
- 360CAS Knee by Kico Knee Innovation Company Pty Ltd