FDA 510(k) Applications Submitted by PROSIE REY-FESSLER
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K000515 |
02/16/2000 |
PRO OSTEON 200R RESORBABLE BONE GRAFT SUBSTITUTE, MODELS 2RG051, 2RG101, 2RG151, 2RG201, 2RG301, 2RG050, 2RG100, 2RG150, |
INTERPORE CROSS INTL. |
| K011148 |
04/16/2001 |
ULTRACONCENTRATOR SYSTEM |
INTERPORE CROSS INTL. |
| K032095 |
07/08/2003 |
INTERPORE CROSS CEMENT RESTRICTOR |
INTERPORE CROSS INTL. |
| K022348 |
07/19/2002 |
ACCESS CONCENTRATION SYSTEM, MODEL ACC-100, ACCESS DISPOSABLE SET, MODEL ADS-2000 |
INTERPORE CROSS INTL. |
| K002592 |
08/21/2000 |
INTERPORE CROSS ANTERIOR CERVICAL PLATE SYSTEM |
INTERPORE CROSS INTL. |
| K993808 |
11/10/1999 |
SYNERGY INTEGRAL SCREWS, MODEL NUMBERS 2161,2162,2163,2164,2165,2166,2167,2168,2169,2210,2211,2212,2215,2216,2217,2220 |
INTERPORE CROSS INTL. |
| K023908 |
11/25/2002 |
INTERPORE CROSS CEMENT RESTRICTOR |
INTERPORE CROSS INTL. |
|
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