Optio-C®
- Primary DI
- 00889024329973
- Brand
- Optio-C®
- Company
- ZIMMER SPINE, INC.
- Model
- 07.01878.006
- Catalog number
- 07.01878.006
- Published
- 2016-06-20
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| OVE | Intervertebral fusion device with integrated fixation, cervical |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00889024329973 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889024329973 | 00889024329973 | 889024329973 | 0889024329973 |
GMDN Terms
| Term | Definition |
|---|---|
| Bone file/rasp, manual | A hand-held manual surgical instrument with a surface(s) of coarse and/or fine grooves or teeth designed to scrape and smooth the surface of bone during a surgical procedure. The device is typically a one-piece instrument with grooves/teeth along all or part of its working end(s). It is available in a variety of sizes and working end designs, including straight and curved ends and often double-ended with a central handle. It is not dedicated for use at a specific anatomy (e.g., sinus, ear) and it is made of metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device. |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts
| Phone | |
|---|---|
| +1(866)774-6368 | zimmer.consumerrelations@zimmerbiomet.com |
Regulatory Flags
- DUNS number
- 787663400
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00889024333499 | Minit® | 300-4018 | 300-4018 | 2015-09-24 |
| 00889024334977 | Sequoia® | 3306-5550 | 3306-5550 | 2015-09-24 |
| 00889024335004 | Sequoia® | 3306-6530 | 3306-6530 | 2015-09-24 |
| 00889024335059 | Sequoia® | 3306-6555 | 3306-6555 | 2015-09-24 |
| 00889024335134 | Sequoia® | 3306-7560 | 3306-7560 | 2015-09-24 |
| 00889024335165 | Sequoia® | 3306-8540 | 3306-8540 | 2015-09-24 |
| 00889024335486 | Sequoia® | 3361-055 | 3361-055 | 2016-06-23 |
| 00889024331419 | InFix® Anterior Lumbar System | 1850-5112 | 1850-5112 | 2016-06-23 |
| 00889024331426 | InFix® Anterior Lumbar System | 1850-5114 | 1850-5114 | 2016-06-23 |
| 00889024331433 | InFix® Anterior Lumbar System | 1850-5308 | 1850-5308 | 2016-06-23 |
| 00889024331440 | InFix® Anterior Lumbar System | 1850-5314 | 1850-5314 | 2016-06-23 |
| 00889024331457 | InFix® Anterior Lumbar System | 1850-5508 | 1850-5508 | 2016-06-23 |
| 00889024331464 | InFix® Anterior Lumbar System | 1850-5512 | 1850-5512 | 2016-06-23 |
| 00889024402577 | InFix® Anterior Lumbar System | 1850-5100 | 1850-5100 | 2016-06-23 |
| 00889024402584 | InFix® Anterior Lumbar System | 1850-5108 | 1850-5108 | 2016-06-23 |
| 00889024402591 | InFix® Anterior Lumbar System | 1850-5110 | 1850-5110 | 2016-06-23 |
| 00889024402607 | InFix® Anterior Lumbar System | 1850-5310 | 1850-5310 | 2016-06-23 |
| 00889024402614 | InFix® Anterior Lumbar System | 1850-5312 | 1850-5312 | 2016-06-23 |
| 00889024402621 | InFix® Anterior Lumbar System | 1850-5510 | 1850-5510 | 2016-06-23 |
| 00889024402638 | InFix® Anterior Lumbar System | 1850-5514 | 1850-5514 | 2016-06-23 |
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| 00810056992958 | aprevo | Carlsmed, Inc. | OVE | 2026-03-17 |
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