Precept

GUDID 00887517344946

PRECEPT Driver, K-Wire

Nuvasive, Inc.

Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Internal spinal fixation procedure kit, reusable Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting

• Primary Device ID: 00887517344946
• NIH Device Record Key: b51edaab-8471-401e-8246-f8ab0e28b0a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Precept
• Version Model Number: 8801002
• Company DUNS: 053950783
• Company Name: Nuvasive, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887517344946 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

[00887517344946]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-10
• Device Publish Date: 2021-08-02

On-Brand Devices [Precept]

• 00887517526533: Precept Extended Taps and Drivers Tray
• 00887517521705: Precept Extended Taps and Drivers Tray
• 00887517521699: Precept Extra Guide and Pile Driver Tray
• 00887517521682: Precept Extra Guide and bull Dozer Tray
• 00887517521644: Precept Reduction XT Set
• 00887517521637: PRECEPT Reduction Implant Set
• 00887517521606: Precept Modular XT Set
• 00887517521583: PRECEPT Modular Configuration
• 00887517521538: Precept MOD - Dismantlable
• 00887517521521: Precept 7.5 Adjunct Tray
• 00887517521071: Precept Open Top Guide Instrument Set
• 00887517515711: PRECEPT Core Clip Ring Implant Set ALPHA
• 00887517491541: PRECEPT Guide, Needle
• 00887517476739: PRECEPT Open Instrument Tray
• 00887517476722: PRECEPT Long Construct Tray
• 00887517476715: PRECEPT Core Instrument Tray 2
• 00887517476708: PRECEPT Core Instrument Tray 1
• 00887517476494: PRECEPT Core Implant Tray
• 00887517453259: PRECEPT Shankdriver, Mod Extended
• 00887517453204: PRECEPT Screwdriver, Reduction Extended
• 00887517451057: ALPHA PRECEPT Extra Guide Set
• 00887517450685: PRECEPT Screw, 6.5x60mm Polyaxial S.R.
• 00887517450678: PRECEPT Screw, 6.5x55mm Polyaxial
• 00887517450661: PRECEPT Screw, 6.5x50mm Polyaxial
• 00887517450654: PRECEPT Screw, 6.5x45mm Polyaxial
• 00887517450647: PRECEPT Screw, 6.5x40mm Polyaxial
• 00887517450630: PRECEPT Screw, 6.5x35mm Polyaxial
• 00887517450623: PRECEPT Screw, 6.5x30mm Polyaxial
• 00887517449795: PRECEPT Screw, 5.5x60mm Polyaxial S.R.
• 00887517449788: PRECEPT Screw, 5.5x55mm Polyaxial
• 00887517449771: PRECEPT Screw, 5.5x50mm Polyaxial
• 00887517449764: PRECEPT Screw, 5.5x45mm Polyaxial
• 00887517449757: PRECEPT Screw, 5.5x40mm Polyaxial
• 00887517449740: PRECEPT Screw, 5.5x35mm Polyaxial
• 00887517449733: PRECEPT Screw, 5.5x30mm Polyaxial
• 00887517449337: PRECEPT Screw, 4.5x60mm Polyaxial S.R.
• 00887517449320: PRECEPT Screw, 4.5x55mm Polyaxial S.R.
• 00887517449313: PRECEPT Screw, 4.5x50mm Polyaxial S.R.
• 00887517449306: PRECEPT Screw, 4.5x45mm Polyaxial
• 00887517449092: PRECEPT Screw, 4.5x40mm Polyaxial
• 00887517449085: PRECEPT Screw, 4.5x35mm Polyaxial
• 00887517449078: PRECEPT Screw, 4.5x30mm Polyaxial
• 00887517449061: PRECEPT Screw, 4.5x25mm Polyaxial
• 00887517431592: PRECEPT Screw, 10.5x120mm Fixed
• 00887517431585: PRECEPT Screw, 10.5x110mm Fixed
• 00887517431578: PRECEPT Screw, 10.5x100mm Fixed
• 00887517431561: PRECEPT Screw, 10.5x90mm Fixed
• 00887517431554: PRECEPT Screw, 10.5x80mm Fixed
• 00887517431547: PRECEPT Screw, 10.5x70mm Fixed
• 00887517431530: PRECEPT Screw, 10.5x60mm Fixed