FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Phoenix Sinus Tarsi Stent System
K Number: K251382
·
Decision Aug 27, 2025
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
1
Review Days
117
Basic Information
- Device Name
- Phoenix Sinus Tarsi Stent System
- K Number
- K251382
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Astra Orthomed, Inc.
- Date Received
- May 2, 2025
- Decision Date
- August 27, 2025
- Product Code
- HWC
- Advisory Committee
- Orthopedic
- Review Advisory Committee
- OR
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HWC | Screw, Fixation, Bone | FDA class 2 | Orthopedic |
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