Medical Device Manufacturer · US , La Jolla , CA

Pillar Surgical, Inc.

5 submissions · 5 cleared · Since 1999

Total

Cleared

Denied

Pillar Surgical, Inc. — FDA 510(k) Submissions

Pillar Surgical, Inc. has submitted 5 FDA 510(k) premarket notifications since 1999, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Malar, Prosthesis, Nose, Internal, Polymer, Ent Synthetic, Porous Polyethylene, Implant, Muscle, Pectoralis, Prosthesis, Chin, Internal . Use the specialty filter in the sidebar to narrow results.

5 devices

1–5 of 5

SILMAX PECTORAL IMPLANT

K002633 · MIC Implant, Muscle, Pectoralis · General & Plastic Surgery

Nov 2000 90d

SILMAX CONTOUR CARVING BLOCK IMPLANT

K002629 · JOF Polymer, Ent Synthetic,... · Ear, Nose, Throat

Nov 2000 89d

PILLAR CHIN IMPLANT

K992239 · FWP Prosthesis, Chin, Internal · General & Plastic Surgery

Nov 1999 143d

PILLAR MALAR IMPLANT

K992240 · LZK Implant, Malar · General & Plastic Surgery

Nov 1999 143d

PILLAR NASAL, DORSAL COLUMELLA AND NASAL DORSUM IMPLANTS

K992242 · FZE Prosthesis, Nose, Internal · General & Plastic Surgery

Nov 1999 143d

Pillar Surgical, Inc.

Pillar Surgical, Inc. — FDA 510(k) Submissions

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