FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FASICULATED NAIL
K Number: K861365
·
Decision May 6, 1986
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
42
Review Days
25
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Basic Information
- Device Name
- FASICULATED NAIL
- K Number
- K861365
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3020
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Applicant
- Lake Region Mfg., Inc.
- Date Received
- April 11, 1986
- Decision Date
- May 6, 1986
- Product Code
- HSB
- 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 |
|---|---|---|---|
| HSB | Rod, Fixation, Intramedullary And Accessories | FDA class 2 | Orthopedic |
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| K080144 | MANDREL GUIDEWIRES OR M-WIRES | Feb 26, 2008 | Substantially Equivalent |
| K073655 | PEGASUS STEERABLE (PTCA) GUIDEWIRE | Jan 28, 2008 | Substantially Equivalent |
| K060454 | TITAN GUIDEWIRE | Mar 24, 2006 | Substantially Equivalent |
| K052347 | TITAN STEERABLE (PTCA) GUIDEWIRE | Feb 17, 2006 | Substantially Equivalent |
| K042338 | CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE | Sep 16, 2004 | Substantially Equivalent |
| K041624 | PTCA STEERABLE HYDROPHILIC GUIDEWIRE | Jul 16, 2004 | Substantially Equivalent |
| K040825 | LAKE REGION HYDROPHILIC GUIDEWIRE | May 17, 2004 | Substantially Equivalent |