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FDA 510(k)

ZIMMER GREAT TOE

K-Number: K823405 · 1983-01-24

ApplicantZimmer, Inc.
Decision Date1983-01-24
Product CodeKWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZIMMER GREAT TOE is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1983-01-24 under 510(k) number K823405. The device is classified under product code KWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZIMMER GREAT TOE?

ZIMMER GREAT TOE is a medical device that received FDA 510(k) clearance on 1983-01-24. The listed applicant is Zimmer, Inc.. The 510(k) number is K823405.

When did ZIMMER GREAT TOE receive FDA 510(k) clearance?

ZIMMER GREAT TOE received FDA 510(k) clearance on 1983-01-24, under 510(k) number K823405.

Who is the listed applicant for ZIMMER GREAT TOE?

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

What is the FDA product code for ZIMMER GREAT TOE?

The FDA product code for ZIMMER GREAT TOE is KWH.

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Other records listing Zimmer, Inc. as applicant

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Related Devices (Code: KWH)

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.

K191966NewPrim SystemBrm ExtremitiesK190136Fusion Silastic SystemFusion Orthopedics, LLCK173491RTS Lesser MTP Implant SystemIn2bones USA, LLCK153609RTS Flexible 1 MPJ Implant w/GrommetsIn2bones USA, LLCK102601ORTHOFLEX RODOrtho-Pro, LLCK023531LESSER METATARSAL PHALANGEAL JOINT IMPLANTNexa Orthopedics, 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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