FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GMK REVISION EXTENSION
K Number: K123721
·
Decision Jul 26, 2013
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
39
Review Days
234
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Basic Information
- Device Name
- GMK REVISION EXTENSION
- K Number
- K123721
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3560
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medacta International
- Date Received
- December 4, 2012
- Decision Date
- July 26, 2013
- Product Code
- JWH
- 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 |
|---|---|---|---|
| JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | FDA class 2 | Orthopedic |
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| K142069 | GMK EXTENSION | Dec 2, 2014 | Substantially Equivalent |
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| K141044 | M.U.S.T. EXTENSION | Aug 18, 2014 | Substantially Equivalent |
| K140826 | GMK SPHERE EXTENSION | Jul 15, 2014 | Substantially Equivalent |