510(k) K931488
K931488 is an FDA 510(k) premarket notification submitted by Franklin Medical USA, Inc. for the device "KSF SPINAL FIXATOR". The FDA issued a decision of SN on January 21, 1994. Franklin Medical USA, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- January 21, 1994
- Date Received
- March 25, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No