U.S. Medical Products, Inc.
Austin, TX, US
U.S. Medical Products, Inc. appears in FDA device records in Austin, TX. FDA records list 24 510(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
- 24
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 24 510(k) clearances for U.S. Medical Products, Inc. between 1992 and 1996. The busiest year on record is 1996, with 10. The most recent is 1996, with 10.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1992 | 1 |
| 1993 | 1 |
| 1994 | 4 |
| 1995 | 8 |
| 1996 | 10 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K962215 | CONSENSUS POSTERIOR STABILIZED KNEE-INTERCONDYLAR NOTCH ROUTER | HWE | Substantially Equivalent | |
| K954818 | CONSENSUS POSTERIOR STABILIZED KNEE | JWH | Substantially Equivalent for Some Indications | |
| K953443 | CONSENSUS PCL SUBSITUTING TIBIAL INSERT | JWH | Substantially Equivalent | |
| K960302 | CONSENSUS ACETABULAR SHELL, ALL UHMWPE | JDI | Substantially Equivalent | |
| K952943 | CONSENSUS ALL POLY TIBIA | JWH | Substantially Equivalent | |
| K960340 | CONSENSUS APEX DOME HOLE PLUG | JDI | Substantially Equivalent | |
| K960339 | CONSENSUS 22MM COCRMO FEMORAL HEAD | JDI | Substantially Equivalent | |
| K960156 | CONSENSUS 32MM COCRMO FEMORAL HEAD | JDI | Substantially Equivalent | |
| K960151 | CONSENSUS 26MM COCRMO FEMORAL HEAD | JDI | Substantially Equivalent | |
| K955386 | CONSENSUS ZIRCONIA FEMORAL HEAD | LZO | Substantially Equivalent for Some Indications | |
| K953792 | CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5 | LZO | Substantially Equivalent for Some Indications | |
| K945589 | CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATE | JWH | Substantially Equivalent | |
| K950013 | CONSENSUS(TM) ORTHOPEDIC DRILL BIT | HWE | Substantially Equivalent | |
| K946197 | CONSENSUS(TM) PATELLA REAMER | HWE | Substantially Equivalent | |
| K944946 | CONSENUS HIP SYSTEM FEMORAL CANAL STARTER REAMER | HWE | Substantially Equivalent | |
| K945208 | CONSENSUS HIP SYSTEM -- TROCHANTERIC CUTTER | HWE | Substantially Equivalent | |
| K945189 | CONSENSUS HIP SYSTEM -- CALCAR PLANER | HWE | Substantially Equivalent | |
| K945186 | CONSENUS HIP SYSTEM -- ACETABULAR REAMER | HWE | Substantially Equivalent | |
| K932837 | CONSENSUS KNEE SYSTEM - PRIMARY KNEE | JWH | Substantially Equivalent for Some Indications | |
| K935193 | CONSENSUS HIP SYSTEM- POROUS COATED TITIANIUM FEMORAL STEM | LZO | Substantially Equivalent for Some Indications | |
| K935453 | CONSENSUS(TM) HIP SYSTEM-HA COATED TIANIUM FEM STEM | MEH | Substantially Equivalent for Some Indications | |
| K933499 | CONSENSUS HIP SYSTEM- NON-POROUS TITANIUM FEMORAL STEM | LZO | Substantially Equivalent | |
| K922561 | CONSENSUS(TM) TOTAL HIP SYSTEM | JDL | Substantially Equivalent | |
| K922560 | CONSENSUS(TM) BIPOLAR SYSTEM | KWY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
- 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
- MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- 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