FDA 510(k) Applications Submitted by WILLIAM E ANSPACH, III
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960514 |
01/25/1996 |
TMP MANDIBULAR COMPRESSION SYSTEM (MODIFICATION) |
ANSPACH FIXATION SYSTEMS |
| K960630 |
02/09/1996 |
ANSPAHC SPEED REDUCER |
THE ANSPACH EFFORT, INC. |
| K011444 |
05/11/2001 |
ANSPACH EMAX DRILL SYSTEM |
THE ANSPACH EFFORT, INC. |
| K955084 |
10/19/1995 |
ASPACH 65,000 (MODIFICATION) |
THE ANSPACH EFFORT, INC. |
| K970530 |
02/12/1997 |
ANSPACH LUBRICATING SYSTEM II |
THE ANSPACH EFFORT, INC. |
| K002903 |
09/18/2000 |
ANSPACH ANGLED MICRONOSE ATTACHMENT |
THE ANSPACH EFFORT, INC. |
| K974025 |
10/23/1997 |
ANSPACH SHIELDED ATTACHMENT |
THE ANSPACH EFFORT, INC. |
| K981688 |
05/11/1998 |
ANSPACH SUTURE ANCHOR |
THE ANSPACH EFFORT, INC. |
| K963686 |
09/12/1996 |
ANSPACH SUTURE ANCHOR (MODIFIED) |
THE ANSPACH EFFORT, INC. |
| K965080 |
12/19/1996 |
ANSPACH MICROMAX SYSTEM |
THE ANSPACH EFFORT, INC. |
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