FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇦 Canada
Signature ONE System
K Number: K232425
·
Decision Dec 12, 2023
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
25
Applicant Total
1
Review Days
123
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Basic Information
- Device Name
- Signature ONE System
- K Number
- K232425
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3660
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Orthosoft Inc. (D/B/A) Zimmer Cas)
- Date Received
- August 11, 2023
- Decision Date
- December 12, 2023
- Product Code
- QHE
- 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 |
|---|---|---|---|
| QHE | Shoulder Arthroplasty Implantation System | FDA class 2 | Orthopedic |
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