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FDA 510(k)

JACOB WIRZ TRANSFIXATION PIN

K-Number: K811209 · 1981-06-16

ApplicantColmed, Ltd.
Decision Date1981-06-16
Product CodeELS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JACOB WIRZ TRANSFIXATION PIN is the device name listed in this FDA 510(k) record. The listed applicant is Colmed, Ltd.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811209. The device is classified under product code ELS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACOB WIRZ TRANSFIXATION PIN?

JACOB WIRZ TRANSFIXATION PIN is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Colmed, Ltd.. The 510(k) number is K811209.

When did JACOB WIRZ TRANSFIXATION PIN receive FDA 510(k) clearance?

JACOB WIRZ TRANSFIXATION PIN received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811209.

Who is the listed applicant for JACOB WIRZ TRANSFIXATION PIN?

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

What is the FDA product code for JACOB WIRZ TRANSFIXATION PIN?

The FDA product code for JACOB WIRZ TRANSFIXATION PIN is ELS.

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Other records listing Colmed, Ltd. 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.

K810636VARIODRAINK810117HALOGEN HEADLIGHT SYSTEMK801208HOLLOW BASKET TITANIUM DENTAL IMPLANTK801006CHARNLEY DESIGN HIP PROSTHESISK800762PS3 TITANIUM SCREW DENTAL IMPLANTK792241PELIMIT

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Related Devices (Code: ELS)

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.

K972985SPLINT ITJeneric/Pentron, Inc.K961704MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEMDentatus USA , Ltd.K922673FLEXIBLE CERAMIC ROPES AND TAPES FOR BONDINGGlasspan, Inc.K834363ENDIX RADICULAR BIOCERAMIC PINC.B.S. Biotechnics, Inc.K801525ZEST ENDODONTIC STABILIZERZest Anchors, 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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