Identity
- Trade Name
- Ablation Platform Mounting Hardware FDA UDI
- Generic Name
- Neurological stereotactic surgery system FDA UDI
- Device Name
- Platform Attachment Set FDA UDI
- Model / Reference
- C0257-00733 FDA UDI
- Description
- Platform Attachment Set FDA UDI
Identifiers
- Catalog Number
- C0257 FDA UDI
- Primary DI / UDI-DI
- 00873263007334 FDA UDI
- 510(k) Number
- K092192 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Neurological stereotactic surgery system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Safe FDA UDI
Category: Neurological stereotactic surgery system
Ablation Platform Mounting Hardware by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K092192 also covers:
- MicroTargeting™ RPD Adapter — FHC, INC.
- MicroTargeting™ Sterilization Basket — FHC, INC.
- OsteoMed™ Manual Driver Handle — FHC, INC.
- WayPoint™ Anchors — FHC, INC.
- WayPoint™ Anchors — FHC, INC.
- WayPoint™ Combination Driver Bit — FHC, INC.
- WayPoint™ Hex Wrench — FHC, INC.
- WayPoint™ Implantation Kit — FHC, INC.
- WayPoint™ Multi-Oblique Platform — FHC, INC.
- WayPoint™ Navigator — FHC, INC.
- WayPoint™ Navigator — FHC, INC.
- WayPoint™ Navigator — FHC, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fhc, Inc.
Sources (1)
- FDA UDI 5b2e78a2-092a-44b1-a0af-071999f9bb2a 36 fields · synced Jun 8, 2026