FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
First Ray Internal Bone Staple System
K Number: K153622
·
Decision Apr 8, 2016
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
4
Review Days
112
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Basic Information
- Device Name
- First Ray Internal Bone Staple System
- K Number
- K153622
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- First Ray, LLC
- Date Received
- December 18, 2015
- Decision Date
- April 8, 2016
- Product Code
- JDR
- 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 |
|---|---|---|---|
| JDR | Staple, Fixation, Bone | FDA class 2 | Orthopedic |
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