Sleds OSN-50
GUDID 00842188109089
Olecranon Sled, 50mm
TRIMED, INCORPORATED
Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable| Primary Device ID | 00842188109089 |
| NIH Device Record Key | f7208095-db77-4505-a9b2-9653f7bae284 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sleds |
| Version Model Number | OSN-50 |
| Catalog Number | OSN-50 |
| Company DUNS | 138041277 |
| Company Name | TRIMED, INCORPORATED |
| 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(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com | |
| Phone | +1(661)255-7406 |
| info@trimedortho.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00842188109089 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K010545
FDA Product Code
| NDL | PIN, FIXATION, SMOOTH, METALLIC |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
Moist Heat or Steam Sterilization
[00842188109089]
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 | 2016-09-07 |
On-Brand Devices [Sleds]
| 00842188109096 | Olecranon Sled, 70mm |
| 00842188109089 | Olecranon Sled, 50mm |
| 00842188109072 | Bent K-Wire 1.6mm |
| 00842188109065 | Medial Malleolar Sled, 60mm |
| 00842188109058 | Medial Malleolar Sled, 42mm |
| 00842188109041 | Medial Malleolar Sled, 35mm |
Trademark Results [Sleds]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SLEDS 78740152 not registered Dead/Abandoned |
Physical Optics Corporation 2005-10-25 |
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