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FDA 510(k)

INTRAMEDULLARY HIP SCREW

K-Number: K895241 · 1990-01-04

ApplicantRichards Medical Co., Inc.
Decision Date1990-01-04
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTRAMEDULLARY HIP SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Richards Medical Co., Inc.. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K895241. 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 INTRAMEDULLARY HIP SCREW?

INTRAMEDULLARY HIP SCREW is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is Richards Medical Co., Inc.. The 510(k) number is K895241.

When did INTRAMEDULLARY HIP SCREW receive FDA 510(k) clearance?

INTRAMEDULLARY HIP SCREW received FDA 510(k) clearance on 1990-01-04, under 510(k) number K895241.

Who is the listed applicant for INTRAMEDULLARY HIP SCREW?

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

What is the FDA product code for INTRAMEDULLARY HIP SCREW?

The FDA product code for INTRAMEDULLARY HIP SCREW is KTT.

Related Clinical Trials

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Other records listing Richards Medical Co., 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.

K896106ROGOZINSKI SPINAL SYSTEM, ADD'L COMPONENTSK900628MODULAR HIP SYSTEMK896580UNI-POLAR HEADK884824TRICON-M TOTAL KNEE SYSTEMK896204ZIRCONIA CERAMIC HEAD ADD'L SIZESK895242PAPPAS TRI-FLANGE VENTILATION TUBE

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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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