FDA 510(k)

STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES

K-Number: K962800 · 1996-09-11

Decision Date1996-09-11

Product CodeHWE

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1996-09-11 under 510(k) number K962800. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES?

STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is Stryker Instruments. The 510(k) number is K962800.

When did STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES receive FDA 510(k) clearance?

STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES received FDA 510(k) clearance on 1996-09-11, under 510(k) number K962800.

Who is the listed applicant for STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES?

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

What is the FDA product code for STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES?

The FDA product code for STRYKER UNIVERSAL DRILL ATTACHMENTS & ACCESSORIES is HWE.

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 Instruments as applicant

K261959Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Push Button Switch (0703-046-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Push Button Switch, Bulk Non-Sterile (0703-046-102);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, 70mm Blade, Rocker Switch (0703-047-100);Neptune® SafeAir® 10ft Smoke Evacuation Pencil, Square Coated, Rocker Switch, Bulk Non-Sterile (0703-047-102)K261544Hydro Irrigation System K253679Hydro Irrigation System K252282SurgiCount+ System K251971RPS Primary TKA Software; RPS Console; RPS Saw One; RPS Cable; RPS Saw Oscillating Tip Cartridge; RPS Console Cart Attachment; Ball Tip Pointer K250483PhotonBlade 3; PhotonBlade 3 Smoke Evacuation

View all 75 devices →

Related Devices (Code: HWE)

K102743ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRESOrtho Solutions Limited K063688SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBEThe Anspach Effort, Inc.K050766EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEMZimmer Trabecular K043310SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEMSynthes (Usa)K022744REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSMedical Device Services K012694REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSAdven Medical

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.