510(k) K071931
K071931 is an FDA 510(k) premarket notification submitted by Codman & Shurtleff, Inc. for the device "CODMAN DISPOSABLE PERFORATOR, MODEL(S) 26-1222, 26-1223". The FDA issued a decision of Substantially Equivalent on October 22, 2007. The device falls under product code HBF (Drills, Burrs, Trephines & Accessories (Compound, Powered)), a Class II device regulated under 21 CFR 882.4305. Codman & Shurtleff, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 22, 2007
- Date Received
- July 13, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Drills, Burrs, Trephines & Accessories (Compound, Powered)
- Device Class
- Class II
- Regulation Number
- 882.4305
- Review Panel
- NE
- Submission Type