MicroTargeting™ RPD Adapter C0255-00731
by Fhc, Inc.
MicroTargeting™ RPD Adapter C0255-00731 is a Class II device made by Fhc, Inc., cleared under FDA 510(k) K092192 on 12 Feb 2010 and listed in FDA GUDID since 29 Feb 2020 (UDI-DI 00873263007310), 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 | Number00873263007310 | Date29 Feb 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK092192 | Date12 Feb 2010 | StatusActive |
Official records
- AccessGUDID record 00873263007310
- FDA 510(k) database K092192
Across registries
- FDA 510(k) K092192 decided 12 Feb 2010 Active
- FDA GUDID UDI-DI 00873263007310 listed 29 Feb 2020 Listed
Timeline
- Cleared FDA 510(k) K092192
- Listed FDA GUDID 00873263007310
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MicroTargeting™ RPD Adapter
- Generic name
- Neurological stereotactic surgery system
- Model / Ref / Catalog
- C0255-00731, C0255
- Primary DI / UDI-DI
- 00873263007310
- 510(k) Number
- FDA product code
- HAW
- GMDN term
- Neurological stereotactic surgery system
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- MRI safety
- MR Safe
- Size
- Outer Diameter — 7.95 MillimeterLumen/Inner Diameter — 2.32 MillimeterLength — 60 Millimeter
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