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FDA 510(k)

MODULAR FLEXIBLE DRILLING SYSTEM

K-Number: K901165 · 1990-06-13

ApplicantDalton Technology, Inc.
Decision Date1990-06-13
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODULAR FLEXIBLE DRILLING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dalton Technology, Inc.. It received FDA 510(k) clearance on 1990-06-13 under 510(k) number K901165. 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 MODULAR FLEXIBLE DRILLING SYSTEM?

MODULAR FLEXIBLE DRILLING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-06-13. The listed applicant is Dalton Technology, Inc.. The 510(k) number is K901165.

When did MODULAR FLEXIBLE DRILLING SYSTEM receive FDA 510(k) clearance?

MODULAR FLEXIBLE DRILLING SYSTEM received FDA 510(k) clearance on 1990-06-13, under 510(k) number K901165.

Who is the listed applicant for MODULAR FLEXIBLE DRILLING SYSTEM?

The FDA 510(k) record lists Dalton Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODULAR FLEXIBLE DRILLING SYSTEM?

The FDA product code for MODULAR FLEXIBLE DRILLING SYSTEM 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.

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Other records listing Dalton Technology, Inc. as applicant

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.

K901166DALTON TECHNOLOGY FLEXIBLE SCREWDRIVER

Related Devices (Code: HWE)

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.

K102743ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRESOrtho Solutions LimitedK063688SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBEThe Anspach Effort, Inc.K050766EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEMZimmer TrabecularK043310SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEMSynthes (Usa)K022744REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSMedical Device ServicesK012694REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSAdven Medical

Official Source

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