Spinery™ RF Ablation System
FDA 510(k) clearance K223303 · decided 2023-08-30
Clearance details
- K-number
- K223303
- Device name
- Spinery™ RF Ablation System
- Applicant
- Axon Spine Medical System
- Decision
- Substantially Equivalent
- Date received
- 2022-10-27
- Decision date
- 2023-08-30
- Days to decision
- 307 days
- Clearance type
- Traditional
- Product code
- GEI
- Device class
- 2
- Regulation number
- 878.4400
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Pompei, IT
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.