Mecron Medical Products, Inc.
Mchenry, IL, US
Mecron Medical Products, Inc. appears in FDA device records in Mchenry, IL. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Mecron Medical Products, Inc. between 1984 and 1986. The busiest year on record is 1985, with 7. The most recent is 1986, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1984 | 6 |
| 1985 | 7 |
| 1986 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K861138 | MASH DERMATOME | GFD | Substantially Equivalent | |
| K854191 | MECRON UNCEMENTED STRUCTURED STEM HIP | Substantially Equivalent | ||
| K844775 | EFFNER-EYE CAUTERY WITH BATTERY HANDLE | HQO | Substantially Equivalent | |
| K844774 | EFFNER FIBER OPTIC CABLES FOR COLD LIGHT TRANSMISS | FCR | Substantially Equivalent | |
| K844488 | MECRON CEMENTED STRUCTURED STEM HIP PROSTHESIS | KWL | Substantially Equivalent | |
| K844487 | MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR | KWL | Substantially Equivalent | |
| K844486 | MECRON MRC-HEADLESS FEMORAL COMPONENT | KWL | Substantially Equivalent | |
| K844773 | EFF-EFFNER BULBS | FFS | Substantially Equivalent | |
| K843449 | AUTODYNAMIC COMPRESSION HIP SCREW-PLATE | KTT | Substantially Equivalent | |
| K843554 | BONE SCREWS | KTW | Substantially Equivalent | |
| K843553 | BONE PLATES | KTW | Substantially Equivalent | |
| K840271 | CEMENTLESS HIP PROSTHESIS | Substantially Equivalent | ||
| K834499 | SHEATHS FOR REINFORCING BONE CEMENT | Substantially Equivalent | ||
| K833881 | ACETABULAR SCREW RING | JDI | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KTWAppliance, Fixation, Nail/Blade/Plate Combination, Single Component
- GFDDermatome
- FFSImage, Illumination, Fiberoptic, For Endoscope
- FCRLight Source, Photographic, Fiberoptic
- KWLProsthesis, Hip, Hemi-, Femoral, Metal
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- HQOUnit, Cautery, Thermal, Ac-Powered
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