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FDA 510(k)

RETROGRADE KNIFE 4MM & 5MM

K-Number: K841974 · 1984-06-19

ApplicantStainless Mfg., Inc.
Decision Date1984-06-19
Product CodeHTZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RETROGRADE KNIFE 4MM & 5MM 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 1984-06-19 under 510(k) number K841974. 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 RETROGRADE KNIFE 4MM & 5MM?

RETROGRADE KNIFE 4MM & 5MM is a medical device that received FDA 510(k) clearance on 1984-06-19. The listed applicant is Stainless Mfg., Inc.. The 510(k) number is K841974.

When did RETROGRADE KNIFE 4MM & 5MM receive FDA 510(k) clearance?

RETROGRADE KNIFE 4MM & 5MM received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841974.

Who is the listed applicant for RETROGRADE KNIFE 4MM & 5MM?

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 RETROGRADE KNIFE 4MM & 5MM?

The FDA product code for RETROGRADE KNIFE 4MM & 5MM 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.

K841980SIDE CUTTING SERRATED BLADEK8419775MM DOUGLE EDGE RING CURETTEK8419712.5MM & 4MM PROBE K841969-LABELINGK841975ROSETTE KNIFE 4MMK841970CAMELBACK HANDLE-K841969-LABELINGK8419814MM & 5MM FILE

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Related Devices (Code: HTZ)

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.

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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