Moss Anchor Set
510(k) K910910
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK910910 | Date24 Jun 1991 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- KNT
- Device Class
- Class II
- Regulation
- 21 CFR Part 876.5980
- Advisory Committee
- Gastroenterology, Urology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 1 Oct 2026
The Moss Anchor Set is a surgical device classified under the product code KNT, intended for use in gastroenterology and urology procedures. It consists of anchors designed to secure components within the body, such as stents or other implants, ensuring stability during and after placement. These anchors are typically used in minimally invasive surgeries to provide a stable fixation point for therapeutic interventions.
The device is supplied sterile and is intended for single-use. It is regulated under FDA 510(k) clearance (K910910) and falls under the advisory committee for Gastroenterology and Urology. The Moss Anchor Set is not MRI-safe, and its use requires adherence to standard surgical protocols. Storage should follow manufacturer guidelines to maintain sterility and functionality.
Other devices from Moss Medical Products
Questions
AI-generated answers, 1 Oct 2026
What is the Moss Anchor Set used for in surgical procedures?
The Moss Anchor Set is designed to provide secure fixation for components like stents or implants during and after placement in minimally invasive surgeries. Its anchors create a stable attachment point, ensuring the device remains properly positioned within the body for therapeutic effectiveness. This is particularly useful in gastroenterology and urology procedures where stability is critical to long-term outcomes.
How is the Moss Anchor Set supplied, and is it reusable?
The Moss Anchor Set is supplied sterile and is intended for single-use only. This ensures patient safety by eliminating the risk of cross-contamination or degradation from repeated sterilization processes. Single-use devices are also designed to maintain consistent performance and reliability for each procedure.
Are there different sizes or models available for the Moss Anchor Set?
The provided data does not specify multiple sizes or models for the Moss Anchor Set. However, the device is tailored for specific applications in gastroenterology and urology, so its design likely aligns with standard fixation requirements for those procedures. For precise sizing or model variations, refer to the manufacturer’s technical documentation or consult with a representative.
How should the Moss Anchor Set be stored to maintain sterility?
The Moss Anchor Set must be stored according to the manufacturer’s guidelines to preserve sterility and functionality. This typically involves keeping the device in its original, sealed packaging in a clean, dry environment, away from direct sunlight or extreme temperatures. Proper storage prevents contamination and ensures the device remains ready for use when needed.
Can the Moss Anchor Set be used in MRI procedures, and what safety precautions should be taken?
The Moss Anchor Set is explicitly not MRI-safe, meaning it should not be used in or near MRI equipment. If MRI imaging is required post-procedure, the device must be removed or alternative imaging modalities must be used. Always follow standard surgical protocols and consult with radiology teams to avoid complications from MRI exposure.