FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Distal Humerus Plating System
K Number: K213895
·
Decision Jan 13, 2022
Classifications
1
FEI Numbers
505
Registration Numbers
505
Same Product Code
1254
Applicant Total
11
Review Days
30
Basic Information
- Device Name
- Distal Humerus Plating System
- K Number
- K213895
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Skeletal Dynamics, Inc.
- Date Received
- December 14, 2021
- Decision Date
- January 13, 2022
- Product Code
- HRS
- 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 |
|---|---|---|---|
| HRS | Plate, Fixation, Bone | FDA class 2 | Orthopedic |
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| K Number | Device Name | ||
|---|---|---|---|
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| K201962 | Skeletal Dynamics Ulnar Shortening Plating System | Oct 13, 2020 | Substantially Equivalent |
| K201662 | REDUCT® Headless Compression Screw System | Jul 16, 2020 | Substantially Equivalent |
| K200538 | Skeletal Dynamics Forearm Plating System | Jun 1, 2020 | Substantially Equivalent |
| K200701 | Skeletal Dynamics Midshaft Humerus Plating System | May 14, 2020 | Substantially Equivalent |
| K200367 | Distal Humerus Plating System | May 14, 2020 | Substantially Equivalent |