Identity
- Trade Name
- RF Stylet FDA UDI
- Generic Name
- Analgesic spinal cord electrical stimulation system FDA UDI
- Device Name
- RF Stylet FDA UDI
- Model / Reference
- MD0528-A FDA UDI
- Description
- RF Stylet FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00818225020068 FDA UDI
- 510(k) Number
- K180981 FDA UDI
- FDA Product Code
- GZB FDA UDI
- GMDN Term
- Analgesic spinal cord electrical stimulation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.5880 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
MR Unsafe FDA UDI
Category: Analgesic spinal cord electrical stimulation system
RF Stylet by Stimwave Technologies Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K180981 also covers:
- 13G Tuohy Needle 4.5" — STIMWAVE TECHNOLOGIES INCORPORATED
- 13G Tuohy Needle 6" — STIMWAVE TECHNOLOGIES INCORPORATED
- Guidewire 3-Pack — STIMWAVE TECHNOLOGIES INCORPORATED
- Introducer 6" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- Large Antenna 30" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- SeaSilk Antenna Large 28" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- SeaSilk Antenna Large 30" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- SeaSilk Antenna Small 12" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- SeaSilk Antenna Small 27" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- Small Antenna 12" Length — STIMWAVE TECHNOLOGIES INCORPORATED
- Small Antenna 27" Length — STIMWAVE TECHNOLOGIES INCORPORATED
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
- Stimwave Technologies Incorporated
Sources (1)
- FDA UDI 92d8d7d2-d4ad-47d6-8950-df8de9961d71 35 fields · synced May 30, 2026