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FDA 510(k)

TWIST LOCK DRILL 1120

K-Number: K831675 · 1983-06-30

ApplicantMicro-Aire Surgical Instruments, Inc.
Decision Date1983-06-30
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TWIST LOCK DRILL 1120 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Aire Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1983-06-30 under 510(k) number K831675. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TWIST LOCK DRILL 1120?

TWIST LOCK DRILL 1120 is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K831675.

When did TWIST LOCK DRILL 1120 receive FDA 510(k) clearance?

TWIST LOCK DRILL 1120 received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831675.

Who is the listed applicant for TWIST LOCK DRILL 1120?

The FDA 510(k) record lists Micro-Aire Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWIST LOCK DRILL 1120?

The FDA product code for TWIST LOCK DRILL 1120 is GET.

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Other records listing Micro-Aire Surgical Instruments, 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.

K904949A.O. SYNTHES,TAP(REPLACEMENT)VARIOUS MODEL NUMBERSK903713OSTEOTOME MODEL NUMBERS 2500-228 & 2500-229K903650OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305K902676MICROGUARD, ORTHOPEDIC PIN PROTECTORSK903664MICRO-AIRE WIRE PASS AND CRANIOTOME DRILLK901967DENDIA WERK BURS AND CUTTING DISCS

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Related Devices (Code: GET)

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.

K960473AESCULAP POWER SYSTEM HANDPIECEAesculap, Inc.K955174SODEM HIGH SPEED SYSTEM FOR NEUROSURGERY & MEDIAN STYERNOTOMYSodem Diffusion SAK942987NUCLEOTOME L KITSurgical Dynamics, Inc.K954076MIDAS REX DRILL ATTACHMENTS & TWIST DRILLSMidas Rex Pneumatic Tools, Inc.K953433MIDAS REX TELESCOPING SYSTEMMidas Rex Pneumatic Tools, Inc.K953432ROTATING, FIXED FOOTED, FIXED SHIELD ATTACHMENTS, DISSECTING TOOLSMidas Rex Pneumatic Tools, Inc.

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.

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