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MENTOR INFLATABLE PENILE PROSTHESIS

FDA premarket approval P000006/S004 · decided 2004-04-28

Approval details

PMA number
P000006
Supplement
S004
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
MENTOR INFLATABLE PENILE PROSTHESIS
Generic name
Device, impotence, mechanical/hydraulic
Applicant
Coloplast Corp.
Date received
2004-04-01
Decision date
2004-04-28
Days to decision
27 days
Decision code
OK30
Product code
FHW
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Plymouth, MN
Statement
CHANGE IN THE RAW MATERIAL SUPPLIER OF A CHEMICAL USED IN THE MANUFACTURING OF MENTOR'S INFLATABLE PENILE PROSTHESIS.

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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