Atlas FDA

CARDIOSEAL

FDA premarket approval P000049/S002 · decided 2002-04-19

Approval details

PMA number
P000049
Supplement
S002
Supplement type
Normal 180 Day Track
Supplement reason
Postapproval Study Protocol
Trade name
CARDIOSEAL
Generic name
Transcatheter septal occluder
Applicant
Nmt Medical, Inc.
Date received
2002-01-11
Decision date
2002-04-19
Days to decision
98 days
Decision code
APPR
Product code
MLV
Advisory committee
Cardiovascular
Expedited review
No
Location
Boston, MA
Statement
APPROVAL FOR THE POST-APPROVAL STUDY PROTOCOL FOR THE CARDIOSEAL SEPTAL OCCLUSION SYSTEM WITH QWIKLOAD.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
NMT MEDICAL TRANSSEPTAL SHEATH SET, MODELS TSS-10-HSC, TSS-11-HSC, TSS12-HSC (K034025)Nmt Medical, Inc.2004-03-26
SPETZLER ROUND HANDLE APPLIERS, MODELS C-3753, C-3753T, C-3754, C-3754T (K994191)Nmt Medical, Inc.2000-02-08