FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NORIAN CRS BONE CEMENT
K Number: K060445
·
Decision Apr 13, 2006
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
43
Applicant Total
402
Review Days
51
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Basic Information
- Device Name
- NORIAN CRS BONE CEMENT
- K Number
- K060445
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5300
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Synthes (Usa)
- Date Received
- February 21, 2006
- Decision Date
- April 13, 2006
- Product Code
- GXP
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| GXP | Methyl Methacrylate For Cranioplasty | FDA class 2 | Neurology |
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Other Clearances by Synthes (Usa)
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|---|---|---|---|
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| K111540 | SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM | Aug 8, 2011 | Substantially Equivalent |
| K110789 | SYNTHES STERNAL ZIPFIX SYSTEM | Jul 28, 2011 | Substantially Equivalent |
| K103002 | SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM | Mar 2, 2011 | Substantially Equivalent |
| K103243 | 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM | Jan 21, 2011 | Substantially Equivalent |
| K102656 | SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM | Dec 20, 2010 | Substantially Equivalent |
| K093299 | SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM | Dec 16, 2010 | Substantially Equivalent |
| K102694 | 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES | Dec 9, 2010 | Substantially Equivalent |
| K100776 | SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM | Aug 3, 2010 | Substantially Equivalent |