FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇮 Finland
ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
K Number: K080879
·
Decision Jun 24, 2008
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
200
Applicant Total
7
Review Days
85
Basic Information
- Device Name
- ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM
- K Number
- K080879
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3040
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- BIORETEC LTD
- Date Received
- March 31, 2008
- Decision Date
- June 24, 2008
- Product Code
- HTY
- 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 |
|---|---|---|---|
| HTY | Pin, Fixation, Smooth | FDA class 2 | Orthopedic |
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Other Clearances by BIORETEC LTD
| K Number | Device Name | ||
|---|---|---|---|
| K130716 | BIORETEC ACTIVASCREW INTERFERENCE | Aug 28, 2013 | Substantially Equivalent |
| K081392 | BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN | Jun 18, 2008 | Substantially Equivalent |
| K072848 | ACTIVASCREW | Nov 2, 2007 | Substantially Equivalent |
| K071863 | ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS) | Aug 31, 2007 | Substantially Equivalent |
| K062980 | ACTIVASCREW | Nov 22, 2006 | Substantially Equivalent |
| K061164 | ACTIVAPIN | Jul 6, 2006 | Substantially Equivalent |