Primary Device ID | 00190376541655 |
NIH Device Record Key | 76922c25-37a7-42a4-924e-95eb34717bf0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ATEC Lateral Navigation Disc Prep Instruments |
Version Model Number | 267-15-000-08-N |
Company DUNS | 602465783 |
Company Name | ALPHATEC SPINE, 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 | false |
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 |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com | |
Phone | +1(760)431-9286 |
Regulatory@alphatecspine.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190376541655 [Primary] |
OLO | Orthopedic stereotaxic instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
[00190376541655]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-26 |
Device Publish Date | 2024-12-18 |
00190376476131 | LIF Nav Primary Dilator Stimulating |
00190376595573 | LIF Navigated Disc Prep |
00190376541686 | LIF NAV, SHAVER 14mm |
00190376541679 | LIF NAV, SHAVER 12mm |
00190376541662 | LIF NAV, SHAVER 10mm |
00190376541655 | LIF NAV, SHAVER 8mm |
00190376541617 | LIF NAV, ENDPLATE SCRAPER SS 10mm |
00190376541594 | LIF NAV, COBB 18mm |
00190376541587 | LIF NAV, COBB 10mm |
00190376541570 | LIF NAV, TRIAL 12 x 18 x 65mm 10° |
00190376541556 | LIF NAV, TRIAL 10 x 18 x 65mm 10° |
00190376541532 | LIF NAV, TRIAL 8 x 18 x 65mm 10° |
00190376541525 | LIF NAV, TRIAL 8 x 18 x 65mm 0° |
00190376541518 | LIF NAV, TRIAL 6 x 18 x 65mm 10° |
00190376541501 | LIF NAV, TRIAL 6 x 18 x 65mm 0° |
00190376541471 | LIF NAV, OSTEOTOME 10mm |
00190376508108 | T-HANDLE, LATCHING, 1/4" HUDSON |