510(k) K953350
K953350 is an FDA 510(k) premarket notification submitted by Medicinelodge, Inc. for the device "MLI INTERFERENCE SCREW". The FDA issued a decision of SN on January 30, 1996. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Medicinelodge, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- January 30, 1996
- Date Received
- July 17, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type