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FDA 510(k)

WARSAW ORTHOPEDIC I BONE PLATE

K-Number: K870727 · 1987-03-09

ApplicantWarsaw Orthopedic, Inc.
Decision Date1987-03-09
Product CodeKTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WARSAW ORTHOPEDIC I BONE PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Warsaw Orthopedic, Inc.. It received FDA 510(k) clearance on 1987-03-09 under 510(k) number K870727. The device is classified under product code KTW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARSAW ORTHOPEDIC I BONE PLATE?

WARSAW ORTHOPEDIC I BONE PLATE is a medical device that received FDA 510(k) clearance on 1987-03-09. The listed applicant is Warsaw Orthopedic, Inc.. The 510(k) number is K870727.

When did WARSAW ORTHOPEDIC I BONE PLATE receive FDA 510(k) clearance?

WARSAW ORTHOPEDIC I BONE PLATE received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870727.

Who is the listed applicant for WARSAW ORTHOPEDIC I BONE PLATE?

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

What is the FDA product code for WARSAW ORTHOPEDIC I BONE PLATE?

The FDA product code for WARSAW ORTHOPEDIC I BONE PLATE is KTW.

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Other records listing Warsaw Orthopedic, 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.

K892877CRADLE, HOSPITAL BED CLOTHINGK883784TSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATEK883783TSRH SACRAL SPINAL SCREWK880211TSRH H/M HOOK HOLDERK880212TSRH H/M HOOK HOLDER W/ROD MOVERK880215TSRH H/M HOOK, EYEBOLT/LOCK NUT ASSEM., SPINAL ROD

View all 24 devices →

Related Devices (Code: KTW)

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.

K182285PK High Tibial Osteotomy Correction SystemPaonan Biotech Co., Ltd.K171606AOS Anterolateral Proximal Humeral PlateAdvanced Orthopaedic Solutions, Inc. (Aos)K170693Phantom Small Bone Intramedullary Nail SystemParagon 28, Inc.K160409AOS Anterolateral Proximal Humeral PlateAdvanced Orthopaedic Solutions, Inc.K122541ORTHOFIX CONTOURS PROIMAL HUMERAL PLATE (PHP)Orthofix SrlK080590AOS PROXIMAL HUMERAL PLATEAdvanced Orthopaedic Solutions, 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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