Company ยท US
Implant Technology, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1995. Name variants (Inc, Corp, punctuation) are merged.
13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented | 6 |
| BTO | Tube, Tracheostomy (W/Wo Connector) | 3 |
| KXA | Prosthesis, Hip, Femoral, Resurfacing | 1 |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 1 |
| LZV | System, Cement Removal Extraction | 1 |
| MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jan 11, 1995 | K921525 | HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESIS Implant Technology, Inc. | LPH |
| May 28, 1992 | K915617 | LSF HA COATED FEMORAL HIP Implant Technology, Inc. | MEH |
| Mar 25, 1992 | K920021 | LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUP Implant Technology, Inc. | JDI |
| Nov 7, 1991 | K913616 | LSF DIAGNOSTIC RELATED GROUP CEMENTED HIP Implant Technology, Inc. | JDI |
| Aug 9, 1990 | K902727 | LSF CEMENTED FEMORAL HIP Implant Technology, Inc. | JDI |
| May 22, 1990 | K901460 | LSF(TM) TOTAL HIP SYSTEM Implant Technology, Inc. | JDI |
| May 2, 1989 | K891472 | IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR Implant Technology, Inc. | LZV |
| Dec 9, 1988 | K884432 | MODIFIED LSF TOTAL HIP SYSTEM Implant Technology, Inc. | JDI |
| Nov 22, 1988 | K883212 | LSF (R) TOTAL HIP SYSTEM - BIPOLAR COMPONENT Implant Technology, Inc. | KXA |
| Jun 11, 1986 | K855017 | LSF* TOTAL HIP SYSTEM Implant Technology, Inc. | JDI |
| Apr 30, 1984 | K841546 | COMMUNI-TRACH TUBE Implant Technology, Inc. | BTO |
| Jul 7, 1983 | K831511 | TRACHEOSTOMY TUBE Implant Technology, Inc. | BTO |
| Jan 8, 1983 | K823291 | COMMUNITRACH TUBE Implant Technology, Inc. | BTO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||