FDA 510(k)

STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT)

K-Number: K111478 · 2011-08-04

Decision Date2011-08-04

Product CodeNKB

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2011-08-04 under 510(k) number K111478. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT)?

STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT) is a medical device that received FDA 510(k) clearance on 2011-08-04. The listed applicant is Stryker Corporation. The 510(k) number is K111478.

When did STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT) receive FDA 510(k) clearance?

STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT) received FDA 510(k) clearance on 2011-08-04, under 510(k) number K111478.

Who is the listed applicant for STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT)?

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT)?

The FDA product code for STRYKER SPINE POWER ADAPTOR (ACCESSORY INSTRUMENT) is NKB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Stryker Corporation as applicant

K232157Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control K212194Stryker Q Guidance System with Cranial Guidance Software, CranialMask Tracker and Microscope Tracker, Passive Optical Navigation Instruments, Mayfield Base with Articulating Arm, and Navigated Biopsy Needle, Electromagnetic Navigation Instruments, Precision Targeting System K223770Sonopet 1Q 3 7cm 1Q Large K221728Aviator® Anterior Cervical Plating (ACP) System, LITe® Plate System, DynaTran™ Anterior Cervical Plating (ACP) System, Reflex™ Hybrid ACP System, UniVise™ Spinous Process Fixation Plate K221074OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device K221098Scopis ENT Software, Scopis ENT Software with TGS, Scopis Planning Software, Electromagnetic Navigation Unit

View all 53 devices →

Related Devices (Code: NKB)

K252139Kentrospine Viktr-MIS® Pedicle screw systemRivarp Medical Pvt., Ltd.K262067iFuse Granite Onyx™ Implant SystemSI-BONE, Inc.K262091FRAXION Spinal Fixation SystemOrtler Global Tibbi Gerecler Anonim Sirketi K262193RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface TechnologyXenix Medical K262828KHEIRON® Spinal Fixation System, including patient specific K-RODS.M.A.I.O K260362QUATTRO Spinal system (Open Configuration); QUATTRO-GADGET Spinal system (MIS Configuration)MANTIZ Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.