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CONFORMIS BICOMPARTMENTAL KNEE REPAIR SYSTEM
Request for Information Form |
Contact Information
|
| Company Name |
CONFORMIS, INC.
|
| Address |
323-C VINTAGE PARK DR.
|
| City, State, Zip |
FOSTER CITY, CA 94404 |
| Country |
US |
| FDA Owner/Operator Phone |
650-286-4151 |
| FDA Medical Specialty Code |
OR - Orthopedic
|
| FDA Product Code |
NPJ |
| FDA Classification Name |
PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| FDA Device Classification Code |
Standards
|
| FDA Regulation Number |
888.3560
|
| FDA Common Generic Name |
BICOMPARTMENTAL KNEE PROSTHESIS |
| FDA Proprietary Device Name |
CONFORMIS BICOMPARTMENTAL KNEE REPAIR SYSTEM |
| FDA Owner / Operator Number |
9058483 |
| FDA Owner / Operator Name |
CONFORMIS, INC. |
| FDA Establishment Registration Number |
3004153240 |
| FDA Registered Establishment Name |
CONFORMIS, INC. |
| FDA Operation Code(s) |
MM - Manufacturer
|
| FDA Listing Date |
02-28-07 |
| FDA Listing Status Code |
Active
|
| Differentiation |
N/A |
| Keywords |
N/A |
| Description |
N/A |
| Brochure |
N/A |
| Product Website
|
N/A |
Competitors of CONFORMIS, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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