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CERAMIC HEAD COMPONENT
Request for Information Form |
Contact Information
|
| Company Name |
BIOMET, INC.
|
| Address |
56 EAST BELL DR. P.O. BOX 587
|
| City, State, Zip |
WARSAW, IN 46581 |
| Country |
US |
| FDA Owner/Operator Phone |
574-267-6639 |
| FDA Medical Specialty Code |
OR - Orthopedic
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| FDA Product Code |
LPF |
| FDA Classification Name |
PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/CERAMIC, CEMENTED |
| FDA Device Classification Code |
Premarket Approval
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| FDA Regulation Number |
NULL
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| FDA Common Generic Name |
CERAMIC HEAD COMPONENT |
| FDA Proprietary Device Name |
CERAMIC HEAD COMPONENT |
| FDA Owner / Operator Number |
1825034 |
| FDA Owner / Operator Name |
BIOMET, INC. |
| FDA Establishment Registration Number |
1825034 |
| FDA Registered Establishment Name |
BIOMET, INC. |
| FDA Operation Code(s) |
MM - Manufacturer
MS - Specification Developer
RR - Repackager/Relabeller
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| FDA Listing Date |
|
| FDA Listing Status Code |
Active
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| Differentiation |
N/A |
| Keywords |
N/A |
| Description |
N/A |
| Brochure |
N/A |
| Product Website
|
N/A |
Competitors of BIOMET, INC.
Our records indicate that the following medical device companies may manufacture a similar device.
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