Ace Orthopedic Manufacturing Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K934962 | AIM SUPRACONDYLAR NAIL | March 22, 1994 |
| K934643 | ACE HUMERAL NAIL | March 22, 1994 |
| K936045 | ACE UNILATERAL FIXATOR II | February 22, 1994 |
| K926047 | ACE 8.0MM CANNULATED CANCELLOUS BONE SCREW | March 31, 1993 |
| K920738 | ACE 100 DEGREES TUBULAR PLATE | July 27, 1992 |
| K813554 | ACE/KYLE CAPTURED HIP SCREW | January 12, 1982 |
| K810193 | TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG | March 20, 1981 |
| K801594 | ACE FISCHER EXTERNAL FIXATION DEVICE | September 9, 1980 |
| K791466 | ACE EXTERNAL BONE CLAMP PART #S11 | August 16, 1979 |
| K781839 | BONE CLAMP, ACE EXTERNAL | November 8, 1978 |
| K781841 | BAR, DISTRACTION | November 8, 1978 |
| K781840 | EXTERNAL ARTICULATION | November 8, 1978 |
| K781251 | THREADED PIN, SELF DRILLING | August 31, 1978 |
| K761229 | ANAL/RECTAL SYRINGE | February 24, 1977 |