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FDA 510(k)

LORENZ STENT

K-Number: K896667 · 1990-02-22

ApplicantWalter Lorenz Surgical, Inc.
Decision Date1990-02-22
Product CodeFWN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LORENZ STENT is the device name listed in this FDA 510(k) record. The listed applicant is Walter Lorenz Surgical, Inc.. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K896667. The device is classified under product code FWN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LORENZ STENT?

LORENZ STENT is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Walter Lorenz Surgical, Inc.. The 510(k) number is K896667.

When did LORENZ STENT receive FDA 510(k) clearance?

LORENZ STENT received FDA 510(k) clearance on 1990-02-22, under 510(k) number K896667.

Who is the listed applicant for LORENZ STENT?

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

What is the FDA product code for LORENZ STENT?

The FDA product code for LORENZ STENT is FWN.

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Other records listing Walter Lorenz Surgical, 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.

K063386LORENZ ORTHODONTIC ANCHORAGE SYSTEMK063052LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATESK063506LORENZ STERNAL CLOSURE SYSTEMK062842TWIST DRILLK061384LORENZ PECTUS SUPPORT BAR, TITANIUM; LORENZ PECTUS SUPPORT BAR STABILIZER, TITANIUMK042516OTOMIMIX

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Related Devices (Code: FWN)

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.

K091135RUTTER SUPRA STOMAL STENTSBoston Medical Products, Inc.K000154ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1E. Benson Hood Lab, Inc.K962693MONTGOMERY RADIOPAQUE LARYNGEAL KEELBoston Medical Products, Inc.K884810SILICONE LARYNGEAL STENTHood LaboratoriesK864936'EXMOOR' DAS GUPTA LARYNGEAL KEELExmoor Plastics , Ltd.K853726LARYNGEALHood Laboratories

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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