Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MENISCAL SAW

K-Number: K800731 · 1980-04-08

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

Device Summary

MENISCAL SAW 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 K800731. 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 MENISCAL SAW?

MENISCAL SAW 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 K800731.

When did MENISCAL SAW receive FDA 510(k) clearance?

MENISCAL SAW received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800731.

Who is the listed applicant for MENISCAL SAW?

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 MENISCAL SAW?

The FDA product code for MENISCAL SAW is HXP.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 19 devices →

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.K800730RETROGRADE KNIFEStainless 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.

↑