MotionLoc® NCB® 02.03161.052
GUDID 00889024083301
Zimmer, Inc.
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile| Primary Device ID | 00889024083301 |
| NIH Device Record Key | 3d5d2bee-caf4-4c7f-89d0-6a3d597dadb2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MotionLoc® NCB® |
| Version Model Number | 02.03161.052 |
| Catalog Number | 02.03161.052 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| 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
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 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 |
| Length | 52 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024083301 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K101696
FDA Product Code
| HWC | Screw, fixation, bone |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
[00889024083301]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2017-09-26 |
On-Brand Devices [MotionLoc® NCB®]
| 00889024083462 | 02.03162.046 |
| 00889024083455 | 02.03162.044 |
| 00889024083448 | 02.03162.042 |
| 00889024083431 | 02.03162.040 |
| 00889024083424 | 02.03162.038 |
| 00889024083417 | 02.03162.036 |
| 00889024083400 | 02.03162.034 |
| 00889024083394 | 02.03162.032 |
| 00889024083387 | 02.03162.030 |
| 00889024083370 | 02.03162.028 |
| 00889024083363 | 02.03162.026 |
| 00889024083356 | 02.03162.024 |
| 00889024083349 | 02.03161.060 |
| 00889024083332 | 02.03161.058 |
| 00889024083325 | 02.03161.056 |
| 00889024083318 | 02.03161.054 |
| 00889024083301 | 02.03161.052 |
| 00889024083295 | 02.03161.050 |
| 00889024083288 | 02.03161.048 |
| 00889024083271 | 02.03161.046 |
| 00889024083264 | 02.03161.044 |
| 00889024083257 | 02.03161.042 |
| 00889024083240 | 02.03161.040 |
| 00889024083233 | 02.03161.038 |
| 00889024083226 | 02.03161.036 |
| 00889024083219 | 02.03161.034 |
| 00889024083202 | 02.03161.032 |
| 00889024083196 | 02.03161.030 |
| 00889024082335 | 02.00024.999 |
Trademark Results [MotionLoc]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MOTIONLOC 77939116 4056959 Live/Registered |
Zimmer, Inc. 2010-02-18 |
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