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FDA 510(k)

BUCKET PROSTHESIS PORP

K-Number: K883727 · 1989-01-13

ApplicantTreace Medical, Inc.
Decision Date1989-01-13
Product CodeETB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BUCKET PROSTHESIS PORP 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 1989-01-13 under 510(k) number K883727. The device is classified under product code ETB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUCKET PROSTHESIS PORP?

BUCKET PROSTHESIS PORP is a medical device that received FDA 510(k) clearance on 1989-01-13. The listed applicant is Treace Medical, Inc.. The 510(k) number is K883727.

When did BUCKET PROSTHESIS PORP receive FDA 510(k) clearance?

BUCKET PROSTHESIS PORP received FDA 510(k) clearance on 1989-01-13, under 510(k) number K883727.

Who is the listed applicant for BUCKET PROSTHESIS PORP?

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 BUCKET PROSTHESIS PORP?

The FDA product code for BUCKET PROSTHESIS PORP is ETB.

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.

K882349MALLET, SURGICALK874779BIPOLATOR 50K873154TREACE MAGNUM OTO-TOOL SYSTEMK872000EYE GARDK870765CANNULATED INSTRUMENT CLEANERSK871706OPTHA PREP

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Related Devices (Code: ETB)

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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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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