Atlas FDA

TITAN INFLATABLE PENILE PROSTHESIS

FDA premarket approval P000006/S045 · decided 2015-11-23

Approval details

PMA number
P000006
Supplement
S045
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
TITAN INFLATABLE PENILE PROSTHESIS
Generic name
Device, impotence, mechanical/hydraulic
Applicant
Coloplast Corp.
Date received
2015-09-21
Decision date
2015-11-23
Days to decision
63 days
Decision code
APPR
Product code
FHW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Plymouth, MN
Statement
APPROVAL FOR CHANGES TO THE HYDROPHILIC COATING SPECIFICATIONS AND MANUFACTURING PROCESS.

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510(k) clearances by this applicant

RecordFirmDate
Heylo™ System (K252140)Coloplast Corp.2025-10-06
Luja Coudé (K251116)Coloplast Corp.2025-06-27
Luja Set (K250270)Coloplast Corp.2025-04-17
SureCath Set (K242049)Coloplast Corp.2024-11-26
Luja Coude (K241210)Coloplast Corp.2024-11-21
Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10, ALXL12) (K242173)Coloplast Corp.2024-11-12
Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562) (K242473)Coloplast Corp.2024-10-18
Folysil Silicone Catheter (K233411)Coloplast Corp.2024-04-15