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FDA 510(k)

TRUE/FLEX METATARSAL RODS

K-Number: K924657 · 1992-11-24

ApplicantApplied Osteo Systems, Inc.
Decision Date1992-11-24
Product CodeKTW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRUE/FLEX METATARSAL RODS is the device name listed in this FDA 510(k) record. The listed applicant is Applied Osteo Systems, Inc.. It received FDA 510(k) clearance on 1992-11-24 under 510(k) number K924657. 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 TRUE/FLEX METATARSAL RODS?

TRUE/FLEX METATARSAL RODS is a medical device that received FDA 510(k) clearance on 1992-11-24. The listed applicant is Applied Osteo Systems, Inc.. The 510(k) number is K924657.

When did TRUE/FLEX METATARSAL RODS receive FDA 510(k) clearance?

TRUE/FLEX METATARSAL RODS received FDA 510(k) clearance on 1992-11-24, under 510(k) number K924657.

Who is the listed applicant for TRUE/FLEX METATARSAL RODS?

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

What is the FDA product code for TRUE/FLEX METATARSAL RODS?

The FDA product code for TRUE/FLEX METATARSAL RODS is KTW.

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Other records listing Applied Osteo Systems, 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.

K935383FEMROD AND FEMROD RECON INSERTK933995TRUE/FLEXTM FEMUR RODS, CAPS, SCREWS AND INSTRUMENTATIONK944501TRUE/FLEX INTRAMEDULLARY ROD END-CAPK941048TRUE/LOK MONOLATERAL/BILATERAL FIXATORK943160INTERFERENCE SCREWK931578TEXAS SCOTTISH RITE EASY/LOCK FIXATOR

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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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