510(k) K121973
K121973 is an FDA 510(k) premarket notification submitted by Biopro, Inc. for the device "BIOPRO HEMI-EDGE TOE SYSTEM". The FDA issued a decision of Substantially Equivalent on October 30, 2012. The device falls under product code KWD (Prosthesis, Toe, Hemi-, Phalangeal), a Class II device regulated under 21 CFR 888.3730. Biopro, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 30, 2012
- Date Received
- July 5, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Toe, Hemi-, Phalangeal
- Device Class
- Class II
- Regulation Number
- 888.3730
- Review Panel
- OR
- Submission Type