(84 days)
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No
The document describes a physical medical device (condom) and its materials, dimensions, and performance testing related to physical properties and biocompatibility. There is no mention of software, algorithms, data processing, or any terms related to AI or ML.
No
The device is primarily used for contraception and preventing the transmission of sexually transmitted infections, which are prophylactic purposes, not therapeutic (treating a disease or condition).
No
Explanation: The device is a condom, used for contraception and preventing STIs, not for diagnosing medical conditions. The provided information focuses on its physical characteristics and biocompatibility, not diagnostic capabilities.
No
The device is a physical condom made of natural rubber latex with lubricant, not a software application.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for contraception and prevention of STIs. This is a physical barrier method used in vivo (on the body), not a test performed in vitro (outside the body) on biological samples to diagnose a condition.
- Device Description: The description details a physical condom, its material, dimensions, and lubricant. This aligns with a medical device used for physical protection, not a diagnostic test kit or instrument.
- Lack of Diagnostic Elements: There is no mention of analyzing biological samples (blood, urine, tissue, etc.), detecting biomarkers, or providing diagnostic information about a patient's health status.
- Performance Studies: The performance studies focus on biocompatibility and physical properties (meeting ASTM standards for condoms), not on diagnostic accuracy metrics like sensitivity, specificity, or AUC.
IVD devices are specifically designed to be used in vitro for the examination of specimens derived from the human body to provide information for diagnostic, monitoring, or compatibility purposes. This device does not fit that description.
N/A
Intended Use / Indications for Use
The Trojan XOXO Thin condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted infections).
Product codes (comma separated list FDA assigned to the subject device)
HIS
Device Description
The Trojan™ XOXO™ Thin Male Natural Rubber Latex Condom with Silicone and Aloe Vera OE Lubricant [Trojan™ XOXO™ Thin condom] is a natural rubber latex sheath, which completely covers the penis with a fitted membrane. A silicone base lubricant containing Aloe Vera OE is applied directly to the condom. The condom is a straight wall nipple end shape consistent with ASTM D3492-08 Standard Specifications for Rubber Contraceptives (Male condom). The Trojan™ XOXO™ Thin condom has a nominal length of 180 ± 10 mm, a nominal thickness of 0.07 ± 0.01 mm, and a nominal flat- width of 52 ±2 mm, measured 30 mm from the open end.
The Trojan™ XOXOTM Thin condom is packaged in a primary foil. Multiple individually foiled condoms may be packaged in a carton.
The Trojan™ XOXO™ Thin condom is a straight wall nipple end condom with lubricant. The predicate and 510(k) subject device are both smooth walled with similar dimensions and contain a silicone based lubricant. The Trojan™ XOXO™ Thin condom is made from a pre-vulcanized natural rubber latex. The purpose and technological function of the pre-vulcanized natural rubber latex in the latex condom formulation is the same as the current natural rubber latex. The Trojan™ XOXO™ Thin condom has an additional ingredient to the silicone based lubricant versus the plain silicone lubricant on the predicate device. This difference does not raise different questions of safety or effectiveness as all condoms must demonstrate biocompatibility and physical testing.
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
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Indicated Patient Age Range
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Intended User / Care Setting
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Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Biocompatibility testing was performed to evaluate the biocompatibility of the Trojan™ XOXO™ Thin condom in accordance with ISO 10993-1. Biological Evaluation of Medical Devices, 2009 and the device is considered safe for consumers based on the results of the biocompatibility testing.
Three (3) lots of Trojan™ XOXO™ Thin condom were tested and met specifications of ASTM D3492-08 Standard Specifications for Rubber Contraceptives (Male Condoms).
The Trojan™ XOXO™ Thin condom has a three year (36 month) shelf-life based on the results of an accelerated stability study protocol created with reference to 21 CFR 801.435. Five year (60 month) expiration dating will be verified with real-time stability according to 21 CFR 801.435.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
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Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
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Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
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§ 884.5300 Condom.
(a)
Identification. A condom is a sheath which completely covers the penis with a closely fitting membrane. The condom is used for contraceptive and for prophylactic purposes (preventing transmission of sexually transmitted infections). The device may also be used to collect semen to aid in the diagnosis of infertility.(b)
Classification. (1) Class II (special controls) for condoms made of materials other than natural rubber latex, including natural membrane (skin) or synthetic.(2) Class II (special controls) for natural rubber latex condoms. The guidance document entitled “Class II Special Controls Guidance Document: Labeling for Natural Rubber Latex Condoms Classified Under 21 CFR 884.5300” will serve as the special control. See § 884.1(e) for the availability of this guidance document.
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Image /page/0/Picture/1 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal features a stylized depiction of three human profiles facing right, arranged in a cascading manner. The profiles are rendered in a dark color, creating a silhouette effect. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the upper portion of the seal.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
August 26, 2016
Church & Dwight Co., Inc. Lisa Burns Manager, Regulatory Affairs 500 Charles Ewing Blvd Ewing, New Jersey 08628
Re: K161545
Trade/Device Name: Trojan™ XOXO™ Thin Male Natural Rubber Latex Condom with Silicone and Aloe Vera OE Lubricant Regulation Number: 21 CFR 884.5300 Regulation Name: Condom Regulatory Class: Class II Product Code: HIS Dated: June 2, 2016 Received: June 3, 2016
Dear Lisa Burns,
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21
1
CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours.
Joyce M. Whang -S
for
Benjamin Fisher, Ph.D. Director Division of Reproductive, Gastro-Renal, and Urological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Indications for Use
510(k) Number (if known) K161545
Device Name
Trojan(TM) XOXO(TM) Thin Male Natural Rubber Latex Condom with Silicone and Aloe Vera OE Lubricant
Indications for Use (Describe)
The Trojan XOXO Thin condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted infections).
| Type of Use (Select one or both, as applicable) |
|---|
| ------------------------------------------------- |
Prescription Use (Part 21 CFR 801 Subpart D)
X Over-The-Counter Use (21 CFR 801 Subpart C)
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II. 510(k) Summary - K161545
| Submitter Name: | Church & Dwight Co., Inc. |
|---|---|
| Submitter Address: | 500 Charles Ewing Boulevard |
| Ewing, NJ 08628 | |
| Contact Person: | Lisa Burns |
| Regulatory Affairs Manager | |
| Church & Dwight Co., Inc. | |
| 469 North Harrison Street | |
| Princeton, NJ 08543 | |
| Tel: (609) 806.1997 | |
| Fax: (609) 403.7411 | |
| Date Prepared: | June 2, 2016 |
| Device Trade Name: | Trojan™ XOXO™ Thin Male Natural Rubber Latex |
| Condom with Silicone and Aloe Vera OE Lubricant | |
| Device Common Name: | Natural Rubber Latex Condom with Lubricant |
| Product Code: | HIS – Condom (21 CFR § 884.5300) |
| Classification: | Class II |
| Predicate Device: | |
| (K912901) | Trojan™ (TM-TBD) Latex Condom with Lubricant |
| [Secondary Brand name HER PLEASURE™ added when | |
| introduced on market] | |
| Indications for Use: | The Trojan XOXO Thin condom is used for |
| contraception and for prophylactic purposes (to help | |
| prevent pregnancy and the transmission of sexually | |
| transmitted infections). |
Device Description:
The Trojan™ XOXO™ Thin Male Natural Rubber Latex Condom with Silicone and Aloe Vera OE Lubricant [Trojan™ XOXO™ Thin condom] is a natural rubber latex sheath, which completely covers the penis with a fitted membrane. A silicone base lubricant containing Aloe Vera OE is applied directly to the condom. The condom is a straight wall nipple end shape consistent with ASTM D3492-08
4
Standard Specifications for Rubber Contraceptives (Male condom). The Trojan™ XOXO™ Thin condom has a nominal length of 180 ± 10 mm, a nominal thickness of 0.07 ± 0.01 mm, and a nominal flat- width of 52 ±2 mm, measured 30 mm from the open end.
The Trojan™ XOXOTM Thin condom is packaged in a primary foil. Multiple individually foiled condoms may be packaged in a carton.
Technological Characteristics:
The Trojan™ XOXO™ Thin condom is a straight wall nipple end condom with lubricant. The predicate and 510(k) subject device are both smooth walled with similar dimensions and contain a silicone based lubricant. The Trojan™ XOXO™ Thin condom is made from a pre-vulcanized natural rubber latex. The purpose and technological function of the pre-vulcanized natural rubber latex in the latex condom formulation is the same as the current natural rubber latex. The Trojan™ XOXO™ Thin condom has an additional ingredient to the silicone based lubricant versus the plain silicone lubricant on the predicate device. This difference does not raise different questions of safety or effectiveness as all condoms must demonstrate biocompatibility and physical testing.
Biocompatibility:
Biocompatibility testing was performed to evaluate the biocompatibility of the Trojan™ XOXO™ Thin condom in accordance with ISO 10993-1. Biological Evaluation of Medical Devices, 2009 and the device is considered safe for consumers based on the results of the biocompatibility testing.
| Test Performed | ISO Standard |
|---|---|
| Cytotoxicity ISO Elution Method | ISO 10993-5 |
| Acute Systemic Toxicity | ISO 10993-11 |
| Primary Rabbit Skin Irritation | ISO 10993-10 |
| Rabbit Vaginal Irritation | ISO 10993-10 |
| Rabbit Penile Irritation | ISO 10993-10 |
| Guinea Pig Maximum Sensitization | ISO 10993-10 |
Physical Testing:
Three (3) lots of Trojan™ XOXO™ Thin condom were tested and met specifications of ASTM D3492-08 Standard Specifications for Rubber Contraceptives (Male Condoms).
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Shelf Life:
The Trojan™ XOXO™ Thin condom has a three year (36 month) shelf-life based on the results of an accelerated stability study protocol created with reference to 21 CFR 801.435. Five year (60 month) expiration dating will be verified with real-time stability according to 21 CFR 801.435.
Substantial Equivalence:
The Trojan™ XOXO™ Thin Condom has the same intended use as the predicate device. Based on performance data and biocompatibility review and testing and safety data, Trojan™ XOXO™ Thin Male Natural Rubber Latex Condom with Silicone and Aloe Vera OE Lubricant is substantially equivalent to the predicate device in technology, intended use, safety and effectiveness.