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FDA 510(k)

MICRO OSCILLATING SAW

K-Number: K811834 · 1981-07-20

ApplicantMicro-Aire Surgical Instruments, Inc.
Decision Date1981-07-20
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO OSCILLATING SAW 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 1981-07-20 under 510(k) number K811834. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO OSCILLATING SAW?

MICRO OSCILLATING SAW is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K811834.

When did MICRO OSCILLATING SAW receive FDA 510(k) clearance?

MICRO OSCILLATING SAW received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811834.

Who is the listed applicant for MICRO OSCILLATING SAW?

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 MICRO OSCILLATING SAW?

The FDA product code for MICRO OSCILLATING SAW is HSZ.

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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: HSZ)

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.

K991588EMS SWISS ORTHOCLAST(Ems Sa) Electro Medical SystemsK972860CURVTEK TSR SYSTEMBiolectron, Inc.K970345ALIGNMENT INSTRUMENTRichard Wolf Medical Instruments Corp.K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.K954080SODEM HIGH SPEED SYSTEMSodem Diffusion SAK944590ETHICON DRILL BIT AND DRILL GUIDEETHICON, 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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