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FDA 510(k)

SIDE CUTTING SERRATED BLADE

K-Number: K841980 · 1984-08-15

ApplicantStainless Mfg., Inc.
Decision Date1984-08-15
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SIDE CUTTING SERRATED BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Stainless Mfg., Inc.. It received FDA 510(k) clearance on 1984-08-15 under 510(k) number K841980. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIDE CUTTING SERRATED BLADE?

SIDE CUTTING SERRATED BLADE is a medical device that received FDA 510(k) clearance on 1984-08-15. The listed applicant is Stainless Mfg., Inc.. The 510(k) number is K841980.

When did SIDE CUTTING SERRATED BLADE receive FDA 510(k) clearance?

SIDE CUTTING SERRATED BLADE received FDA 510(k) clearance on 1984-08-15, under 510(k) number K841980.

Who is the listed applicant for SIDE CUTTING SERRATED BLADE?

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

What is the FDA product code for SIDE CUTTING SERRATED BLADE?

The FDA product code for SIDE CUTTING SERRATED BLADE is HTZ.

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Other records listing Stainless Mfg., 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.

K8419775MM DOUGLE EDGE RING CURETTEK8419814MM & 5MM FILEK841975ROSETTE KNIFE 4MMK841970CAMELBACK HANDLE-K841969-LABELINGK8419712.5MM & 4MM PROBE K841969-LABELINGK841974RETROGRADE KNIFE 4MM & 5MM

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Related Devices (Code: HTZ)

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K933933CEBOPLANESynvasive Technology, Inc.K931737HEDLEYL INTRAMEDULLARY PREPARATION BRUSHSynvasive Technology, Inc.K87088245 DEGREE SHAVERBowen & Company, Inc.K853678KAMBIN SPINAL INSTRUMENT SETPilling Co.K850527ARTHROSCOPY SUCTION BIOPSY PUNCHT. Korossurgical Instruments Corp.K850423CONCEPT SUCTION SLEEVEConcept, 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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