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FDA 510(k)

RETROGRADE KNIFE

K-Number: K800730 · 1980-04-08

ApplicantStainless Mfg., Inc.
Decision Date1980-04-08
Product CodeHXP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RETROGRADE KNIFE 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 1980-04-08 under 510(k) number K800730. The device is classified under product code HXP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETROGRADE KNIFE?

RETROGRADE KNIFE is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is Stainless Mfg., Inc.. The 510(k) number is K800730.

When did RETROGRADE KNIFE receive FDA 510(k) clearance?

RETROGRADE KNIFE received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800730.

Who is the listed applicant for RETROGRADE KNIFE?

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?

The FDA product code for RETROGRADE KNIFE is HXP.

Related Clinical Trials

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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 CURETTEK841975ROSETTE KNIFE 4MMK841970CAMELBACK HANDLE-K841969-LABELINGK8419712.5MM & 4MM PROBE K841969-LABELINGK8419814MM & 5MM FILE

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Related Devices (Code: HXP)

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.

K872858WILLIAMS VERTEBRAL SPREADERAce Medical Co.K800732MENISCOTOMEStainless Mfg., Inc.K800731MENISCAL SAWStainless Mfg., Inc.K800733DOUBLE-EDGE CURETTEStainless Mfg., 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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