510(k) K011460
K011460 is an FDA 510(k) premarket notification submitted by Biopro, Inc. for the device "WUJIN #3 TIBIAL BONE PLATE". The FDA issued a decision of Substantially Equivalent on August 7, 2001. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Biopro, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 7, 2001
- Date Received
- May 11, 2001
- 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