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FDA 510(k)

CANNON NASAL SPLINT

K-Number: K863382 · 1986-10-07

ApplicantTreace Medical, Inc.
Decision Date1986-10-07
Product CodeEPP
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CANNON NASAL SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Treace Medical, Inc.. It received FDA 510(k) clearance on 1986-10-07 under 510(k) number K863382. The device is classified under product code EPP. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNON NASAL SPLINT?

CANNON NASAL SPLINT is a medical device that received FDA 510(k) clearance on 1986-10-07. The listed applicant is Treace Medical, Inc.. The 510(k) number is K863382.

When did CANNON NASAL SPLINT receive FDA 510(k) clearance?

CANNON NASAL SPLINT received FDA 510(k) clearance on 1986-10-07, under 510(k) number K863382.

Who is the listed applicant for CANNON NASAL SPLINT?

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

What is the FDA product code for CANNON NASAL SPLINT?

The FDA product code for CANNON NASAL SPLINT is EPP.

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.

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Other records listing Treace Medical, 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.

K883727BUCKET PROSTHESIS PORPK882349MALLET, SURGICALK874779BIPOLATOR 50K873154TREACE MAGNUM OTO-TOOL SYSTEMK872000EYE GARDK870765CANNULATED INSTRUMENT CLEANERS

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Related Devices (Code: EPP)

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.

K942158AQUAPLAST NASAL SPLINTS, PRECUT SILVER SPLINT PATTERNS AND SPLINT KITSWfr/Aquaplast Corp.K942724EXTERNAL NASAL SPLINTMicromed Development Corp.K895502MICROTEK REUTER-STYLE BI-VALVE INTRANASAL SPLINTMicrobio-Medics, Inc.K890599HOOD NASAL SPLINTHood LaboratoriesK882244RICHARDS THERMOPLASTIC DORSAL NASAL SPLINTRichards Medical Co., Inc.K872905AMERICAN NASAL SPONGEAmerican Silk Sutures, 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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