FDA 510(k) Applications Submitted by PAUL GASSER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K960398 |
01/29/1996 |
STERI-OSS APICAL IMPLANT |
STERI-OSS, INC. |
K980439 |
02/04/1998 |
REPLACE CYLINDRICAL IMPLANTS |
STERI-OSS, INC. |
K960886 |
03/04/1996 |
STERI-OSS 6 MM DIAMETER HA COATED IMPLANTS |
STERI-OSS, INC. |
K960979 |
03/11/1996 |
SCREW EXTRACTION DEVICE AND THREAD CLEANING TAP |
STERI-OSS, INC. |
K961020 |
03/12/1996 |
STERI-OSS 6MM DIAMETER TPS COATED IMPLANTS |
STERI-OSS, INC. |
K962120 |
05/31/1996 |
TOMOGRAPH ACCESSORIES |
STERI-OSS, INC. |
K962844 |
07/22/1996 |
REPLACE TPS COATED IMPLANTS |
STERI-OSS, INC. |
K962845 |
07/22/1996 |
REPLACE HA COATED IMPLANTS |
STERI-OSS, INC. |
K963121 |
08/12/1996 |
FIXTURE MOUNT KIT |
STERI-OSS, INC. |
K963401 |
08/29/1996 |
TPS APICAL IMPLANT |
STERI-OSS, INC. |
K964220 |
10/22/1996 |
REPLACE TITANIUM IMPLANT SYSTEM |
STERI-OSS, INC. |
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