ACE-FISCHER®BAYONET POINT WIRE
- Primary DI
- 00887868001512
- Brand
- ACE-FISCHER®BAYONET POINT WIRE
- Company
- Biomet Orthopedics, LLC
- Model
- 10469
- Catalog number
- 10469
- Published
- 2015-10-24
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K083789 | 000 | ACE FISCHER EXTERNAL FIXATION SYSTEM | DePuy Orthopaedics, Inc. | 2009-03-23 | KTT |
| K112218 | 000 | ACE-FISCHER(R), TEMPFIX(R), HOFFMAN CLASSIC(TM) EXTERNAL FIXATORS | DePuy Orthopaedics, Inc. | 2011-12-15 | KTT |
| K895079 | 000 | ACE BEADED K-WIRES ACE OLIVE WIRES | Buckman Co., Inc. | 1989-09-13 | HTY |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887868001512 | Primary | GS1 | 0 | |
| 70887868001511 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887868001512 | 00887868001512 | 887868001512 | 0887868001512 |
| 70887868001511 | 70887868001511 |
GMDN Terms#
| Term | Definition |
|---|---|
| External orthopaedic fixation system, single-use, non-sterile | An assembly of non-sterile devices designed to stabilize fractured bones to promote treatment and healing. It typically consists of an external plastic and/or metallic fixator (a framework) and other external and/or implantable components such as clamps, rods, rings, pins, bolts, and nuts, as well as some reusable instrumentation (e.g., wrenches, depth gauge, tensioner). It is used mainly to help the healing of long bones such as the femur, tibia and humerus, as well as fractures of the foot and ankle, joint fusions, and limb lengthening. This is a single-use device intended to be sterilized prior to use. |
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
- 3
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887868494758 | Vanguard® Instruments | 32-486259 | 32-486259 | 2022-05-25 |
| 00888480584162 | PRO OSTEON 200 | 2B040 | 2B040 | 2015-10-24 |
| 00888480584179 | PRO OSTEON 200 | 2B045 | 2B045 | 2015-10-24 |
| 00888480584186 | PRO OSTEON 200 | 2B075 | 2B075 | 2015-10-24 |
| 00888480584247 | PRO OSTEON 200 | 2G02 | 2G02 | 2015-10-24 |
| 00888480584254 | PRO OSTEON 200 | 2G05 | 2G05 | 2015-10-24 |
| 00888480584339 | PRO OSTEON 200R | 2RG005 | 2RG005 | 2015-10-24 |
| 00888480584346 | PRO OSTEON 200R | 2RG02 | 2RG02 | 2015-10-24 |
| 00888480584353 | PRO OSTEON 200R | 2RG05 | 2RG05 | 2015-10-24 |
| 00888480584360 | PRO OSTEON 200R | 2RG15 | 2RG15 | 2015-10-24 |
| 00888480584476 | PRO OSTEON 500 | 5B040 | 5B040 | 2015-10-24 |
| 00888480584483 | PRO OSTEON 500 | 5B075 | 5B075 | 2015-10-24 |
| 00888480584490 | PRO OSTEON 500 | 5B100 | 5B100 | 2015-10-24 |
| 00888480584575 | PRO OSTEON 500 | 5G05 | 5G05 | 2015-10-24 |
| 00888480584582 | PRO OSTEON 500 | 5G10 | 5G10 | 2015-10-24 |
| 00888480584599 | PRO OSTEON 500 | 5G15 | 5G15 | 2015-10-24 |
| 00888480584629 | PRO OSTEON 500 | 5G30 | 5G30 | 2015-10-24 |
| 00888480584681 | PRO OSTEON 500R | 5RB010 | 5RB010 | 2015-10-24 |
| 00888480584698 | PRO OSTEON 500R | 5RB014 | 5RB014 | 2015-10-24 |
| 00888480584704 | PRO OSTEON 500R | 5RB024 | 5RB024 | 2015-10-24 |
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