REACH MODULAR HIP SYSTEM
- Primary DI
- 00880304282124
- Brand
- REACH MODULAR HIP SYSTEM
- Company
- Biomet Orthopedics, LLC
- Model
- 21-108399
- Catalog number
- 21-108399
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K022463 | 000 | HA MODULAR REACH PROXIMAL POROUS AND HA MODULAR REACH COLLARED PROXIMAL POROUS FEMORAL STEMS | Biomet Orthopedics, Inc. | 2002-08-16 | LPH |
| K030055 | 000 | MALLORY/HEAD TOTAL HIP SYSTEM; HA MALLORY/HEAD TOTAL HIP SYSTEM; BI-METRIC FEMORAL COMPONENTS | Biomet, Inc. | 2003-08-11 | LPH |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00880304282124 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00880304282124 | 00880304282124 | 880304282124 | 0880304282124 |
GMDN Terms#
| Term | Definition |
|---|---|
| Uncoated knee femur prosthesis, metallic | An implantable device designed to replace the femoral condyles (femoral component) during primary bicondylar replacement of the knee joint, femoral bone resection, or to replace a dysfunctional knee prosthesis (revision); it is made of metal [e.g., cobalt-chrome (Co-Cr), cobalt-chrome-molybdenum (Co-Cr-Mo), titanium (Ti)] and is not coated with a material intended to improve fixation and stability by promoting bone ingrowth. The device is designed to articulate with tibial and, if required, patellar prosthetic components of the knee joint and its implantation is intended to be performed with bone cement. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00880304533424 | DVR® CrosslockWIDE PLATE RIGHT (HEAD WIDTH x OVERALL LENGTH) | 131813050 | 131813050 | 2015-10-24 |
| 00889024707726 | SolidLok® | 2810-01-021 | 281001021 | 2026-06-10 |
| 00887868561368 | VersaNail® | 2810-13-037 | 281013037 | 2023-09-07 |
| 00889024707061 | A.L.P.S.® | 2142-35-007 | 214235007 | 2026-05-11 |
| 00889024707078 | DRILL BIT | 231200201 | 231200201 | 2026-05-11 |
| 00889024707085 | DRILL BIT | 8290-29-070 | 829029070 | 2026-05-11 |
| 00880304410541 | FIBER OPTICS FOR RC RETRACTOR | 908534 | 908534 | 2019-06-11 |
| 00880304321946 | BIFURCATED FIBER OPTIC CABLE | 31-555502 | 31-555502 | 2017-07-28 |
| 00880304463912 | 4MM X 9FT. LIGHT CABLE | 906117 | 906117 | 2017-07-28 |
| 00889024707054 | CALIBRATED DRILL BIT | 2142-27-070 | 214227070 | 2026-04-27 |
| 00880304233102 | Biomet® Knee System | 141872 | 141872 | 2015-10-24 |
| 00880304233126 | Biomet® Knee System | 141874 | 141874 | 2015-10-24 |
| 00880304233140 | Biomet® Knee System | 141876 | 141876 | 2015-10-24 |
| 00880304233164 | Biomet® Knee System | 141878 | 141878 | 2015-10-24 |
| 00880304233171 | Biomet® Knee System | 141880 | 141880 | 2015-10-24 |
| 00880304233188 | Biomet® Knee System | 141882 | 141882 | 2015-10-24 |
| 00880304433403 | Vanguard® Knee System | 184144 | 184144 | 2015-10-24 |
| 00880304433410 | Vanguard® Knee System | 184181 | 184181 | 2015-10-24 |
| 00880304433564 | Vanguard® Knee System | 184285 | 184285 | 2015-10-24 |
| 00880304433984 | Vanguard® Knee System | 184280 | 184280 | 2015-10-24 |
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