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FDA 510(k)

K-CAP-I ORTHOPEDIC FIXATION WIRE CAP

K-Number: K902053 · 1990-09-14

ApplicantWestcon Orthopedics, Inc.
Decision Date1990-09-14
Product CodeLYT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

K-CAP-I ORTHOPEDIC FIXATION WIRE CAP 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 1990-09-14 under 510(k) number K902053. The device is classified under product code LYT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the K-CAP-I ORTHOPEDIC FIXATION WIRE CAP?

K-CAP-I ORTHOPEDIC FIXATION WIRE CAP is a medical device that received FDA 510(k) clearance on 1990-09-14. The listed applicant is Westcon Orthopedics, Inc.. The 510(k) number is K902053.

When did K-CAP-I ORTHOPEDIC FIXATION WIRE CAP receive FDA 510(k) clearance?

K-CAP-I ORTHOPEDIC FIXATION WIRE CAP received FDA 510(k) clearance on 1990-09-14, under 510(k) number K902053.

Who is the listed applicant for K-CAP-I ORTHOPEDIC FIXATION WIRE CAP?

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-CAP-I ORTHOPEDIC FIXATION WIRE CAP?

The FDA product code for K-CAP-I ORTHOPEDIC FIXATION WIRE CAP is LYT.

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, STERILEK901525K-CAPE ORTHOPEDIC WIRES AND PINS

Related Devices (Code: LYT)

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.

K040363CERAMIC TIPPED SKULL PINThe Jerome Group, Inc.K983685BONE BANDChapel and Assoc.K980594OSTEONICS FX-CABLELOK GRIP COMPONENTSOsteonics Corp.K914812K-CAP-E, STERILEWestcon Orthopedics, Inc.K912762K-CAP-I, STERILEWestcon Orthopedics, Inc.K902676MICROGUARD, ORTHOPEDIC PIN PROTECTORSMicro-Aire Surgical Instruments, 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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