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)

ARTHROPHONOMETER

K-Number: K862286 · 1987-01-07

ApplicantArthrotek, Inc.
Decision Date1987-01-07
Product CodeNFQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ARTHROPHONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Arthrotek, Inc.. It received FDA 510(k) clearance on 1987-01-07 under 510(k) number K862286. The device is classified under product code NFQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROPHONOMETER?

ARTHROPHONOMETER is a medical device that received FDA 510(k) clearance on 1987-01-07. The listed applicant is Arthrotek, Inc.. The 510(k) number is K862286.

When did ARTHROPHONOMETER receive FDA 510(k) clearance?

ARTHROPHONOMETER received FDA 510(k) clearance on 1987-01-07, under 510(k) number K862286.

Who is the listed applicant for ARTHROPHONOMETER?

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

What is the FDA product code for ARTHROPHONOMETER?

The FDA product code for ARTHROPHONOMETER is NFQ.

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 Arthrotek, 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.

K061776ARTHROTEK MAXFIRE MENISCAL REPAIR DEVICEK0618012.8 & 3.5MM LACTOSCREW SUTURE ANCHORSK061657HITCH LACTOSORB SUTURE ANCHORK061389ALLTHREAD LACTOSORB SUTURE ANCHORK060693MICROSTRIKE AND ALLTHREAD PEEK SUTURE ANCHORK053461EZLOC FEMORAL FIXATION DEVICE

View all 17 devices →

Related Devices (Code: NFQ)

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.

K970116ESG-1 ELECTROSONOGRAM (ESG-1)Myo-Tronics, Inc.K905657SONOPAK/QS, SONOPAKBioresearchK905449ELECTROSONOGRAM ESG-1Myo-Tronics, 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.

↑