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TOROSA TESTICULAR PROSTHESIS

FDA premarket approval P020003/S007 · decided 2010-11-10

Approval details

PMA number
P020003
Supplement
S007
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
TOROSA TESTICULAR PROSTHESIS
Generic name
Prosthesis, testicular
Applicant
Coloplast Corp.
Date received
2010-08-18
Decision date
2010-11-10
Days to decision
84 days
Decision code
APPR
Product code
FAF
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Plymouth, MN
Statement
APPROVAL FOR THE CHANGE OF THE SALINE FILLED TESTICULAR PROSTHESIS AND THE RE-BRANDING TO ¿TOROSA TESTICULAR 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