510(k) K181653
K181653 is an FDA 510(k) premarket notification submitted by Ethicon Endo-Surgery, LLC for the device "Ethicon Circular Stapler, Ethicon Circular Stapler -XL Sealed". The FDA issued a decision of Substantially Equivalent on Sep 18, 2018. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Ethicon Endo-Surgery, LLC has 183 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 18, 2018
- Date Received
- Jun 22, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4750
- Review Panel
- SU
- Submission Type
- 510(k)