510(k) K800502
K800502 is an FDA 510(k) premarket notification submitted by Richard F. Kronner, M.D. for the device "ADDITIONAL COMPONENTS KRONNER COMPRES". The FDA issued a decision of Substantially Equivalent on April 2, 1980. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Richard F. Kronner, M.D. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 2, 1980
- Date Received
- March 4, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plate, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type