Dow Corning Wright
Dow Corning Wright appears in FDA public data with 0 recalls, 74 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 7, 1994.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 74
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K932210 | ORTHOLOC ADVANTIM REVISION FEMORAL COMPONENT | September 7, 1994 |
| K932911 | ORTHOLOC ADVANTIM L.S. TIBIAL COMPONENT | June 30, 1994 |
| K934354 | LACEY ALL POLYETHYLENE TIBIAL COMPONENT | June 3, 1994 |
| K932222 | SLT FEMORAL HEAD | May 27, 1994 |
| K932858 | ORTHOLOC ADVANTIM TIBIAL BASE COMPONENT | February 16, 1994 |
| K930228 | ORTHOLOC ADVANTIM TIBIAL STEM 5 DEGREE | November 30, 1993 |
| K925900 | LACEY REVISION FEMORAL COMPONENT | August 24, 1993 |
| K930189 | ORTHOLOC(R) ADVANTIM(TM) POSTERIOR STAB FEMOR COMP | August 6, 1993 |
| K930188 | ORTHOLOC(R) ADVANTIM(TM) FEMORAL COMPONENT | August 3, 1993 |
| K930190 | ORTHOLOC(R) ADVANTIM(TM) NON-POR COAT FEMOR COMP | August 2, 1993 |
| K926257 | ORTHOLOC ADVANTIM THICK TIBIAL BASE COMPONENT | May 18, 1993 |
| K915525 | WHITESIDE ORTHOLOC(R) MODULAR REVISION FEMOR COMP | May 5, 1993 |
| K920969 | HYDROXYLAPATITE INFINITY(R) | May 5, 1993 |
| K920968 | INFINITY(R) COLLARLESS/MICROTAPER TROCHANTERIC MOD | May 5, 1993 |
| K920929 | POLY INSERT 20 DEGREE | May 5, 1993 |
| K925512 | CERAMIC FEMORAL HEAD-28MM LONG, MODIFICATION | February 12, 1993 |
| K920593 | CERAMIC FEMORAL HEAD | August 31, 1992 |
| K915448 | CORTICAL BONE SCREW | February 28, 1992 |
| K915238 | TRAC-WRIGHT TRAC 10 CATHETER | February 19, 1992 |
| K915350 | HYDROXYAPATITE INFINITY TROCHANTERIC MODULE | February 3, 1992 |