FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DEPUY SYNTHES MAXFRAME AUTOSTRUT System
K Number: K231922
·
Decision Jul 26, 2023
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
19
Review Days
27
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Basic Information
- Device Name
- DEPUY SYNTHES MAXFRAME AUTOSTRUT System
- K Number
- K231922
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- DePuy Synthes
- Date Received
- June 29, 2023
- Decision Date
- July 26, 2023
- Product Code
- KTT
- 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 |
|---|---|---|---|
| KTT | Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component | FDA class 2 | Orthopedic |
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