Skip to content

Costasis/Dynastat Surgical Hemostats

by Angiotech Medical Device Technologies

PMA P990030

Withdrawn Withdrawn in United States.

Was authorized under PMA, withdrawn

Ended

Withdrawn 13 Jun 2000

PMA

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA PMA, synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPWD Approval withdrawn NumberP990030 Date13 Jun 2000Approval withdrawnStatusWithdrawn

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Withdrawn

Specification

PMA

Trade Name
Vitagel Surgical Hemostat
Generic Name
Absorbable collagen hemostatic agent with thrombin
PMA Number
FDA Product Code
PMX
Device Class
Class III
Regulation
21 CFR Part 878.4490
Advisory Committee
General, Plastic Surgery
FDA Decision
APWD Approval withdrawn

Other devices from Angiotech Medical Device Technologies