ACE-FISCHER®5MM HALF PIN FF1016020
GUDID 00887868071164
Biomet Orthopedics, LLC
External orthopaedic fixation system, single-use, non-sterile External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use External orthopaedic fixation system, single-use| Primary Device ID | 00887868071164 |
| NIH Device Record Key | 1cf201a1-fe22-486d-a31b-5d39c3e7e5df |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ACE-FISCHER®5MM HALF PIN |
| Version Model Number | FF-10160.20 |
| Catalog Number | FF1016020 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868071164 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K083789
FDA Product Code
| KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
[00887868071164]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
On-Brand Devices [ACE-FISCHER®5MM HALF PIN]
| 00887868071799 | FS-10220.80 |
| 00887868071782 | FS-10210.70 |
| 00887868071775 | FS-10200.60 |
| 00887868071768 | FS-10190.50 |
| 00887868071751 | FS-10185.45 |
| 00887868071744 | FS-10180.40 |
| 00887868071737 | FS-10175.35 |
| 00887868071720 | FS-10170.30 |
| 00887868071713 | FS-10165.25 |
| 00887868071706 | FS-10160.20 |
| 00887868071690 | FS-10155.15 |
| 00887868071683 | FS-10150.10 |
| 00887868071256 | FF-10220.80 |
| 00887868071249 | FF-10210.70 |
| 00887868071232 | FF-10200.60 |
| 00887868071225 | FF-10190.50 |
| 00887868071218 | FF-10185.45 |
| 00887868071201 | FF-10180.40 |
| 00887868071195 | FF-10175.35 |
| 00887868071188 | FF-10170.30 |
| 00887868071171 | FF-10165.25 |
| 00887868071164 | FF-10160.20 |
| 00887868071157 | FF-10155.15 |
| 00887868071140 | FF-10150.10 |
Trademark Results [ACE-FISCHER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ACE-FISCHER 73421065 1281428 Live/Registered |
Ace Orthopedic Company, Inc. 1983-04-11 |
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