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FDA 510(k)

SUTTER FINGER JOINT PROSTHESIS

K-Number: K870200 · 1987-10-09

ApplicantSutter Biomedical, Inc.
Decision Date1987-10-09
Product CodeKYJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SUTTER FINGER JOINT PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Sutter Biomedical, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K870200. 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 SUTTER FINGER JOINT PROSTHESIS?

SUTTER FINGER JOINT PROSTHESIS is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Sutter Biomedical, Inc.. The 510(k) number is K870200.

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

SUTTER FINGER JOINT PROSTHESIS received FDA 510(k) clearance on 1987-10-09, under 510(k) number K870200.

Who is the listed applicant for SUTTER FINGER JOINT PROSTHESIS?

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

What is the FDA product code for SUTTER FINGER JOINT PROSTHESIS?

The FDA product code for SUTTER FINGER JOINT PROSTHESIS is KYJ.

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Other records listing Sutter Biomedical, 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.

K875249SUTTER PHALANGEAL CAPK861983SUTTER LESSER METATARSAL CAPK850274SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENTK830974SUTTER CPM 5000K830649SUTTER CPM 2000K823539SUTTER CPM

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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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