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FDA 510(k)

REPLACEMENT SAW BLADES FOR STRYKER AIR

K-Number: K820601 · 1982-03-23

Decision Date1982-03-23
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT SAW BLADES FOR STRYKER AIR 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 1982-03-23 under 510(k) number K820601. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT SAW BLADES FOR STRYKER AIR?

REPLACEMENT SAW BLADES FOR STRYKER AIR is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is Micro-Aire Surgical Instruments, Inc.. The 510(k) number is K820601.

When did REPLACEMENT SAW BLADES FOR STRYKER AIR receive FDA 510(k) clearance?

REPLACEMENT SAW BLADES FOR STRYKER AIR received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820601.

Who is the listed applicant for REPLACEMENT SAW BLADES FOR STRYKER AIR?

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 REPLACEMENT SAW BLADES FOR STRYKER AIR?

The FDA product code for REPLACEMENT SAW BLADES FOR STRYKER AIR is GFA.

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.

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.

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Related Devices (Code: GFA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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