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FDA 510(k)

DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR

K-Number: K890989 · 1990-04-05

ApplicantOrigin Medsystems, Inc.
Decision Date1990-04-05
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1990-04-05 under 510(k) number K890989. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR?

DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR is a medical device that received FDA 510(k) clearance on 1990-04-05. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K890989.

When did DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR receive FDA 510(k) clearance?

DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR received FDA 510(k) clearance on 1990-04-05, under 510(k) number K890989.

Who is the listed applicant for DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR?

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

What is the FDA product code for DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR?

The FDA product code for DR. HERZBERG DISPOSABLE EXTERNAL FIXATOR is KTT.

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Other records listing Origin Medsystems, Inc. as applicant

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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