FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INTERPORE CROSS CEMENT RESTRICTOR
K Number: K032095
·
Decision Aug 8, 2003
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
53
Applicant Total
39
Review Days
31
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Basic Information
- Device Name
- INTERPORE CROSS CEMENT RESTRICTOR
- K Number
- K032095
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.3300
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Interpore Cross Intl.
- Date Received
- July 8, 2003
- Decision Date
- August 8, 2003
- Product Code
- JDK
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| JDK | Prosthesis, Hip, Cement Restrictor | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Interpore Cross Intl.
| K Number | Device Name | ||
|---|---|---|---|
| K050861 | PEEK CAS | May 27, 2005 | Substantially Equivalent |
| K031399 | INTERGRO DBM | Feb 18, 2005 | Substantially Equivalent |
| K041407 | TITANIUM MESH IMPLANT | Dec 29, 2004 | Substantially Equivalent |
| K043229 | MODIFICATION TO ALTIUS OCT SYSTEM | Dec 21, 2004 | Substantially Equivalent |
| K042798 | C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM | Nov 4, 2004 | Substantially Equivalent |
| K040928 | EXPANDABLE PEEK VBR IMPLANT | Aug 27, 2004 | Substantially Equivalent |
| K041794 | C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM | Jul 19, 2004 | Substantially Equivalent |
| K041449 | SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT | Jul 1, 2004 | Substantially Equivalent |
| K033961 | ALTIUS OCT SYSTEM | Apr 14, 2004 | Substantially Equivalent |
| K040168 | MODIFICATION TO GEO STRUCTURE | Apr 8, 2004 | Substantially Equivalent |