FDA 510(k) Applications Submitted by SARA BAILEY SHULTZ
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K011451 |
05/11/2001 |
REUNITE FUSION SCREW |
BIOMET, INC. |
| K021254 |
04/19/2002 |
LACTOSORB MINI INTERFERENCE SCREW |
BIOMET ORTHOPEDICS, INC. |
| K021260 |
04/19/2002 |
REDUCED SIZE ONCOLOGY SALVAGE SYSTEM |
BIOMET, INC. |
| K021828 |
06/04/2002 |
SMALL HAMMER TOE PIN |
BIOMET, INC. |
| K021832 |
06/04/2002 |
ARTHROTEK RESORBABLE NO-PROFILE LACTOSORB L-15 SCREW & WASHER |
BIOMET, INC. |
| K012469 |
08/02/2001 |
RESORBABLE NO PROFILE SCREW AND WASHER |
BIOMET MANUFACTURING, INC. |
| K012503 |
08/03/2001 |
METAL SCREW ANCHOR |
BIOMET MANUFACTURING, INC. |
| K012569 |
08/09/2001 |
MODIFICATION TO: INJECTABLE MIMIX |
BIOMET, INC. |
| K012572 |
08/09/2001 |
SOFT TISSUE SCREW AND WASHER |
BIOMET, INC. |
| K012872 |
08/27/2001 |
RESORBABLE SCREW ANCHOR |
ARTHROTEK, INC. |
| K013042 |
09/10/2001 |
DISCOVERY ELBOW |
BIOMET ORTHOPEDICS, INC. |
| K013534 |
10/23/2001 |
SELF-COUNTERSINKING BONE SCREW |
BIOMET ORTHOPEDICS, INC. |
| K014305 |
12/31/2001 |
RESORBABLE LACTOSORB-L ACL CROSSPIN |
ARTHROTEK, INC. |
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