Medical Device Manufacturer · US , Rockville , MD

Sts Biopolymers

1 submissions · 1 cleared · Since 1999

Total

Cleared

Denied

Sts Biopolymers — FDA 510(k) Submissions

Sts Biopolymers has submitted 1 FDA 510(k) premarket notifications since 1999, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Percutaneous, Biopsy . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

ECHO-COAT ULTRASOUND NEEDLES

K983647 · MJG Device, Percutaneous, Biopsy · General & Plastic Surgery

Jan 1999 96d

Sts Biopolymers

Sts Biopolymers — FDA 510(k) Submissions

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