DISCOVERY ELBOW
FDA 510(k) clearance K013042 · decided 2001-10-10
Clearance details
- K-number
- K013042
- Device name
- DISCOVERY ELBOW
- Applicant
- Biomet Orthopedics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2001-09-10
- Decision date
- 2001-10-10
- Days to decision
- 30 days
- Clearance type
- Special
- Product code
- JDC
- Device class
- 2
- Regulation number
- 888.3150
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Warsaw, IN, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
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| DISCOVERY ELBOW - X-SMALL (K090473) | Biomet Manufacturing Corp | 2009-03-25 |
| ACCLAIM TOTAL ELBOW SYSTEM (K060696) | DePuy Orthopaedics, Inc. | 2006-04-14 |
| COONRAD/MORREY TOTAL ELBOW, MODEL 8105 SERIES (K053189) | Zimmer, Inc. | 2005-12-09 |
| POROUS COATED DISCOVERY ELBOW (K051975) | Biomet, Inc. | 2005-09-06 |
| LPS UPPER EXTREMITY (K042664) | Depuy, Inc. | 2004-12-08 |
| COONRAD/MORREY ELBOW CEMENT RESTRICTOR (K040389) | Zimmer, Inc. | 2004-05-17 |
| DISCOVERY ELBOW-MOSAIC DISTAL HUMERAL REPLACEMENT SYSTEM (K033280) | Biomet, Inc. | 2003-12-19 |