Pillar Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pillar Surgical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pillar Surgical, Inc. has 5 FDA 510(k) cleared medical devices. Based in La Jolla, US.
Historical record: 5 cleared submissions from 1999 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pillar Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pillar Surgical, Inc.
5 devices
Cleared
Nov 21, 2000
SILMAX PECTORAL IMPLANT
General & Plastic Surgery
90d
Cleared
Nov 20, 2000
SILMAX CONTOUR CARVING BLOCK IMPLANT
Ear, Nose, Throat
89d
Cleared
Nov 22, 1999
PILLAR CHIN IMPLANT
General & Plastic Surgery
143d
Cleared
Nov 22, 1999
PILLAR MALAR IMPLANT
General & Plastic Surgery
143d
Cleared
Nov 22, 1999
PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS
General & Plastic Surgery
143d