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FDA 510(k)

1.1 SCREWDRIVERS

K-Number: K872490 · 1987-07-23

ApplicantMicro-Aire Surgical Instruments, Inc.
Decision Date1987-07-23
Product CodeLRZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

1.1 SCREWDRIVERS 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 1987-07-23 under 510(k) number K872490. The device is classified under product code LRZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1.1 SCREWDRIVERS?

1.1 SCREWDRIVERS is a medical device that received FDA 510(k) clearance on 1987-07-23. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K872490.

When did 1.1 SCREWDRIVERS receive FDA 510(k) clearance?

1.1 SCREWDRIVERS received FDA 510(k) clearance on 1987-07-23, under 510(k) number K872490.

Who is the listed applicant for 1.1 SCREWDRIVERS?

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 1.1 SCREWDRIVERS?

The FDA product code for 1.1 SCREWDRIVERS is LRZ.

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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 & 2500-229K902676MICROGUARD, ORTHOPEDIC PIN PROTECTORSK903650OSCILLATING SAW BLADES # SO-305,MO-305 AND ZO-305K903664MICRO-AIRE WIRE PASS AND CRANIOTOME DRILLK901967DENDIA WERK BURS AND CUTTING DISCS

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Related Devices (Code: LRZ)

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.

K896589MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERPOptikK872387STANDARD SCREW DRIVERMed-Tool, 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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