FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MENDEC SPINE
K Number: K042415
·
Decision Jun 9, 2005
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
107
Applicant Total
14
Review Days
275
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Basic Information
- Device Name
- MENDEC SPINE
- K Number
- K042415
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3027
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tecres S.P.A.
- Date Received
- September 7, 2004
- Decision Date
- June 9, 2005
- Product Code
- NDN
- 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 |
|---|---|---|---|
| NDN | Cement, Bone, Vertebroplasty | FDA class 2 | Orthopedic |
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