AVS Anchor-L
- Primary DI
- 07613252602835
- Brand
- AVS Anchor-L
- Company
- Stryker Corporation
- Model
- 48992020
- Catalog number
- 48992020
- Device description
- ALL IN ONE GUIDE
- Published
- 2016-09-24
- 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
Product Codes
| Code | Name |
|---|---|
| MAX | Intervertebral fusion device with bone graft, lumbar |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07613252602835 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07613252602835 | 07613252602835 | 7613252602835 |
GMDN Terms
| Term | Definition |
|---|---|
| Orthopaedic fixation implant alignment tool | A surgical instrument designed to facilitate the correct orientation (alignment) of an orthopaedic fixation implant, implants, or system of implants during orthopaedic surgery. It may be used, e.g., to align a series of bone screws in an implant system for posterior stabilization of the spine, or to align a spinal anatomical fixation implant. It is available in a variety of shapes and sizes and allows the surgeon to engage this device with the implant(s) and align them in the desired configuration. It is typically made of high-grade stainless steel or titanium alloy and will have profiled features to fit into the implant(s) to align them. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Height | 20 | Millimeter |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 149183167
- 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
- true
- 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 |
|---|---|---|---|---|
| 07613327687637 | N/A | 6517040016 | 6517-040-016 | 2026-03-19 |
| 07613327687644 | N/A | 6517040010 | 6517-040-010 | 2026-03-19 |
| 07613327687651 | N/A | 6517070021 | 6517-070-021 | 2026-03-19 |
| 07613327687668 | N/A | 6517048021 | 6517-048-021 | 2026-03-19 |
| 07613327687675 | N/A | 6517040012 | 6517-040-012 | 2026-03-19 |
| 07613327628357 | RPS | 8808000000 | 8808-000-000 | 2025-10-01 |
| 07613327656763 | BPX | 7900012000 | 7900-012-000 | 2026-03-04 |
| 07613327656770 | BPX | 7900013000 | 7900-013-000 | 2026-03-04 |
| 07613327657760 | BPX | 7900034000 | 7900-034-000 | 2026-03-04 |
| 07613327657777 | BPX | 7900015000 | 7900-015-000 | 2026-03-04 |
| 07613327657784 | BPX | 7900031000 | 7900-031-000 | 2026-03-04 |
| 07613327657791 | BPX | 7900099000 | 7900-099-000 | 2026-03-04 |
| 07613327657807 | N/A | 7900376010 | 7900-376-010 | 2026-03-04 |
| 07613327657814 | BPX | 7900037000 | 7900-037-000 | 2026-03-04 |
| 07613327657821 | N/A | 7900377010 | 7900-377-010 | 2026-03-04 |
| 07613327657838 | N/A | 7900378010 | 7900-378-010 | 2026-03-04 |
| 07613327659429 | BPX | 7900025000 | 7900-025-000 | 2026-03-04 |
| 37613327693288 | Malis | 6760-180-010 | 6760-180-010-Z01 | 2026-02-25 |
| 37613327693295 | Malis | 6760-180-005 | 6760-180-005-Z01 | 2026-02-25 |
| 37613327693363 | Malis | 6760-180-015 | 6760-180-015-Z01 | 2026-02-25 |
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| 00840283403224 | LumiVy™ | VY SPINE LLC | MAX | 2026-03-24 |
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