Joint Medical Products Corp.
Mchenry, IL, US
Joint Medical Products Corp. appears in FDA device records in Mchenry, IL. FDA records list 33 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 33
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 33 510(k) clearances for Joint Medical Products Corp. between 1984 and 1996. The busiest year on record is 1992, with 5. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 1 |
| 1985 | 3 |
| 1986 | 1 |
| 1987 | 2 |
| 1988 | 1 |
| 1989 | 1 |
| 1990 | 3 |
| 1991 | 4 |
| 1992 | 5 |
| 1993 | 1 |
| 1994 | 4 |
| 1995 | 5 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K955511 | ARTHOPOR I & II ACETABULAR CUP/ARTHOPOR II OBLONG ACETABULAR CUP | LPH | Substantially Equivalent | |
| K954935 | S-ROM FEMORAL HIP STEM - SIZE 14 X 8 | LPH | Substantially Equivalent | |
| K944321 | S-ROM NOILES POSTERIOR STABILIZED TOTAL KNEE SYSTEM II | JWH | Substantially Equivalent for Some Indications | |
| K951726 | S-ROM ZTP UHMWPE ACETABULAR CUP | JDI | Substantially Equivalent | |
| K951084 | S-ROM OPC (ONE-PIECE CEMENTED) II FEMORAL HIP PROSTHESIS | JDI | Substantially Equivalent | |
| K951000 | ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM | LPH | Substantially Equivalent | |
| K941769 | KNEE PROTHESIS | JWH | Substantially Equivalent for Some Indications | |
| K936037 | S-ROM NOILES CRUCIATE RETAINING KNEE | JWH | Substantially Equivalent for Some Indications | |
| K934412 | COATED ZT PROXIMAL SLEEVE | LPH | Substantially Equivalent | |
| K931676 | S-ROM(R) ZTT(TM) ACETABULAR CUP-APICAL HOLE PLUG | JDL | Substantially Equivalent | |
| K935078 | S-ROM TOTAL HIP REPLACEMENT SYSTEM | JDG | Substantially Equivalent for Some Indications | |
| K924940 | FEMORAL & TIBIAL AUGMENT BLOCK | JWH | Substantially Equivalent for Some Indications | |
| K924492 | POLY-DIAL INSERTS | LPH | Substantially Equivalent for Some Indications | |
| K920739 | S-ROM TOTAL HIP REPLACEMENT SYSTEM | JDI | Substantially Equivalent for Some Indications | |
| K921111 | S-ROM ZIRCONIA CERMAMIC FEMORAL HEAD | LZO | Substantially Equivalent | |
| K922824 | KNEE JT. PATELLO FEMORO TIBIAL POLYMER/METAL/POLYM | HSX | Substantially Equivalent | |
| K920317 | S-ROM LF FEMORAL HEAD | JDI | Substantially Equivalent | |
| K912713 | S-ROM ZT HA PROXIMAL FEMORAL SLEEVE | MEH | Substantially Equivalent for Some Indications | |
| K913231 | S-ROM(TM) TOTAL LHIP SYSTEM W/CERAMIC HEAD | JDI | Substantially Equivalent | |
| K905810 | NOILES(TM) TOTAL KNEE PROSTHESIS, MODIFICATION | JWH | Substantially Equivalent | |
| K905258 | S-ROM OBLONG ACETABULAR CUP | JDI | Substantially Equivalent | |
| K904746 | S-ROM(TM) FEMORAL STEM CENTRALIZER/CEMENT SPACER | JDK | Substantially Equivalent | |
| K896048 | S-ROM/NOILES MARK 3 | KRO | Substantially Equivalent | |
| K896397 | S-ROM(TM)/NOILES(TM) MARK 5 KNEE | JWH | Substantially Equivalent for Some Indications | |
| K893584 | GRIPPER II ACETABULAR CUP | LWJ | Substantially Equivalent for Some Indications | |
| K870088 | S-ROM SUPERCUP ACETABULAR CUP | LWJ | Substantially Equivalent for Some Indications | |
| K870730 | NOILES TOTAL KNEE PROSTHESIS | JWH | Substantially Equivalent | |
| K870271 | S-ROM POLY-DIAL CONSTRAINED SOCKET FOR ACET. CUP | KWZ | Substantially Equivalent for Some Indications | |
| K860207 | S-ROM 135 POROUS COATED FEMORAL STEM COLLAR | Substantially Equivalent for Some Indications | ||
| K844050 | ARTHOPOR-ACETABULAR COMPONENT | JDI | Substantially Equivalent for Some Indications | |
| K851422 | S-ROM 135 FEMORAL STEM & COLLAR(PART OF S-ROM HIP | JDI | Substantially Equivalent | |
| K851421 | S-ROM ACETABULAR CUP(PART OF S-ROM 135TM TOTAL HIP | LPH | Substantially Equivalent | |
| K841022 | SRC TOTAL KNEE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- JDKProsthesis, Hip, Cement Restrictor
- KWZProsthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
- JDGProsthesis, Hip, Femoral Component, Cemented, Metal
- JDLProsthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- LWJProsthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
- MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain