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FDA 510(k)

K-CAPE ORTHOPEDIC WIRES AND PINS

K-Number: K901525 · 1990-04-23

ApplicantWestcon Orthopedics, Inc.
Decision Date1990-04-23
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

K-CAPE ORTHOPEDIC WIRES AND PINS is the device name listed in this FDA 510(k) record. The listed applicant is Westcon Orthopedics, Inc.. It received FDA 510(k) clearance on 1990-04-23 under 510(k) number K901525. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-CAPE ORTHOPEDIC WIRES AND PINS?

K-CAPE ORTHOPEDIC WIRES AND PINS is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is Westcon Orthopedics, Inc.. The 510(k) number is K901525.

When did K-CAPE ORTHOPEDIC WIRES AND PINS receive FDA 510(k) clearance?

K-CAPE ORTHOPEDIC WIRES AND PINS received FDA 510(k) clearance on 1990-04-23, under 510(k) number K901525.

Who is the listed applicant for K-CAPE ORTHOPEDIC WIRES AND PINS?

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

What is the FDA product code for K-CAPE ORTHOPEDIC WIRES AND PINS?

The FDA product code for K-CAPE ORTHOPEDIC WIRES AND PINS is KTT.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Westcon Orthopedics, 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.

K914812K-CAP-E, STERILEK912762K-CAP-I, STERILEK902053K-CAP-I ORTHOPEDIC FIXATION WIRE CAP

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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