OrthoView 7.3.1
by Meridian Technique Limited 2 variants
OrthoView 7.3.1 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Meridian Technique Limited, cleared under FDA 510(k) K063327 on 22 Nov 2006 and listed in FDA GUDID since 28 Nov 2018 (UDI-DI B021731WINWK0), active as of 23 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 | NumberB021731WINWK0 | Date28 Nov 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK063327 | Date22 Nov 2006 | StatusActive |
Official records
- FDA 510(k) database K063327
Across registries
- FDA 510(k) K063327 decided 22 Nov 2006 Active
- FDA GUDID UDI-DI B021731WINWK0 listed 28 Nov 2018 Listed
Timeline
- Cleared FDA 510(k) K063327
- Listed FDA GUDID B021731WINWK0
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- OrthoView
- Generic name
- Orthopaedic/craniofacial implantation planning software
- Model / reference
- 7.3.1
- Primary DI / UDI-DI
- B021731WINWK0
- 510(k) Number
- FDA product code
- LLZ
- GMDN term
- Orthopaedic/craniofacial implantation planning software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Orthopaedic/craniofacial implantation planning software.