Response Navigation 01-1800-6022
Response Navigation 01-1800-6022 is a Class II device made by Orthopediatrics Corp., cleared under FDA 510(k) K203573 on 4 Feb 2021 and listed in FDA GUDID since 24 Feb 2021 (UDI-DI 00841132181133), 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 | Number00841132181133 | Date24 Feb 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK203573 | Date4 Feb 2021 | StatusActive |
Official records
- AccessGUDID record 00841132181133
- FDA 510(k) database K203573
Across registries
- FDA 510(k) K203573 decided 4 Feb 2021 Active
- FDA GUDID UDI-DI 00841132181133 listed 24 Feb 2021 Listed
Timeline
- Cleared FDA 510(k) K203573
- Listed FDA GUDID 00841132181133
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Response Navigation
- Generic name
- Abdominal/ENT/orthopaedic surgical probe, reusable
- Model / Ref / Catalog
- 01-1800-6022
- Primary DI / UDI-DI
- 00841132181133
- 510(k) Number
- FDA product code
- OLO
- GMDN term
- Abdominal/ENT/orthopaedic surgical probe, reusable
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Abdominal/ENT/orthopaedic surgical probe, reusable.