Trestle Luxe
- Primary DI
- 00844856001107
- Brand
- Trestle Luxe
- Company
- ALPHATEC SPINE, INC.
- Model
- 61545-010
- Device description
- FIXED ANGLE SELF-TAPPING SCREW - 4.5MMX10MM
- Published
- 2015-08-01
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K102820 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00844856001107 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00844856001107 | 00844856001107 | 844856001107 | 0844856001107 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic fixation plate kit, non-bioabsorbable, sterile | A sterile collection of small sheets of firm material and bone screws intended to be implanted onto fractured bone fragments to bridge and stabilize the fracture gap, and shield the site from stress as the bone heals; the components are made of a material that is not chemically degraded or absorbed by natural body processes (includes implant grade metal such as surgical steel, titanium alloy, or carbon fibre). Tools for implantation may be included. The device is typically used to treat traumatic or pathological orthopaedic fractures; it may also be used to temporarily augment bone following a lengthening procedure, or for arthrodesis (joint fusion). |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 10 | Millimeter |
| Outer Diameter | 4.5 | Millimeter |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(760)431-9286 | Regulatory@alphatecspine.com |
Regulatory Flags#
- DUNS number
- 602465783
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
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| 00190376529189 | ATEC Posterior Navigation Disc Prep Instruments | 244-01-000-12-N | 2024-04-20 | |
| 00190376476162 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-08-N | 2023-08-26 | |
| 00190376476179 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-10-N | 2023-08-26 | |
| 00190376476186 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-12-N | 2023-08-26 | |
| 00190376522906 | ATEC Lateral Navigation Disc Prep Instruments | 266-01-000-14-N | 2023-08-26 | |
| 00840180512395 | General Instruments | CI-11129-3424 | 2026-05-15 | |
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