510(k) K851122
K851122 is an FDA 510(k) premarket notification submitted by Surgeons Choice, Inc. for the device "PI-PNEUMO INTESTINAL STAPLING CARTRIDGE". The FDA issued a decision of Substantially Equivalent on April 25, 1985. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Surgeons Choice, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 25, 1985
- Date Received
- March 19, 1985
- 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