FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CinchLock Flex Knotless Suture Anchor
K Number: K151314
·
Decision Jul 23, 2015
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
3
Review Days
66
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Basic Information
- Device Name
- CinchLock Flex Knotless Suture Anchor
- K Number
- K151314
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pivot Medical
- Date Received
- May 18, 2015
- Decision Date
- July 23, 2015
- Product Code
- MBI
- 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 |
|---|---|---|---|
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue | FDA class 2 | Orthopedic |
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