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FDA 510(k)

FINGER JOINT PROSTHESIS

K-Number: K013629 · 2002-01-25

ApplicantAvanta Orthopaedics, Inc.
Decision Date2002-01-25
Product CodeKYJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FINGER JOINT PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Avanta Orthopaedics, Inc.. It received FDA 510(k) clearance on 2002-01-25 under 510(k) number K013629. The device is classified under product code KYJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER JOINT PROSTHESIS?

FINGER JOINT PROSTHESIS is a medical device that received FDA 510(k) clearance on 2002-01-25. The listed applicant is Avanta Orthopaedics, Inc.. The 510(k) number is K013629.

When did FINGER JOINT PROSTHESIS receive FDA 510(k) clearance?

FINGER JOINT PROSTHESIS received FDA 510(k) clearance on 2002-01-25, under 510(k) number K013629.

Who is the listed applicant for FINGER JOINT PROSTHESIS?

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

What is the FDA product code for FINGER JOINT PROSTHESIS?

The FDA product code for FINGER JOINT PROSTHESIS is KYJ.

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Other records listing Avanta Orthopaedics, 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.

K030881AVANTA CARPAL FUSION PLATING SYSTEMK021859WRIST IMPLANTK023604MODIFICATION TO RADIAL HEAD IMPLANTK011819RADIAL HEAD IMPLANTK010847K'FIXK003033SCAPHIX, STAPLE, FIXATION, BONE

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Related Devices (Code: KYJ)

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.

K233670Ascension Silicone MCP; Ascension Silicone PIPAscension Orthopedics, Inc.K220142BRM Digitalis SpacerBrm Extremities SrlK211385KeriFlex® MCP and PIP Finger Joint ProsthesesKeri Medical SAK083107MODIFICATION TO DEPUY NEUFLEX PIP FINGERDePuy Orthopaedics, Inc.K082231ASCENSION SILICONE PIPAscension Orthopedics, Inc.K022892ASCENSION SILLICONE MCPAscension 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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