PYE — Staple Removal Kit Class I
FDA product code PYE covers "Staple Removal Kit", a Class I medical device regulated under 21 CFR 878.4760. Submissions are reviewed by the General, Plastic Surgery panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- PYE
- Device Class
- Class I
- Regulation Number
- 878.4760
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Definition
This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K844110 | pelco | XTRACETEZE SURGICAL SKIN STAPLE REMOVER 2001 | November 19, 1984 |