A.L.P.S.®
- Primary DI
- 00887868457906
- Brand
- A.L.P.S.®
- Company
- Biomet Orthopedics, LLC
- Model
- 110016937
- Catalog number
- 110016937
- Published
- 2020-11-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HRS | Plate, fixation, bone |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HRS | Plate, Fixation, Bone | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K132898 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887868457906 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887868457906 | 00887868457906 | 887868457906 | 0887868457906 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)348-9500 | customerservice@zimmerbiomet.com |
Regulatory Flags#
- DUNS number
- 129278169
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- 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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