Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT

K-Number: K973406 · 1997-12-08

ApplicantOsteonics Corp.
Decision Date1997-12-08
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Osteonics Corp.. It received FDA 510(k) clearance on 1997-12-08 under 510(k) number K973406. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT?

OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT is a medical device that received FDA 510(k) clearance on 1997-12-08. The listed applicant is Osteonics Corp.. The 510(k) number is K973406.

When did OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT receive FDA 510(k) clearance?

OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT received FDA 510(k) clearance on 1997-12-08, under 510(k) number K973406.

Who is the listed applicant for OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT?

The FDA 510(k) record lists Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT?

The FDA product code for OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT is JWH.

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 Osteonics Corp. 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.

K983657OSTEONICS SERIES 7000 AD TIBIAL TRAYK980070OSTEONICS HA-COATED DEVICESK984375OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLYK982798OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEMK984585OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVEK990203OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS

View all 178 devices →

Related Devices (Code: JWH)

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.

K262057GMK ExtensionMedacta International SAK260063GSPE SpacerThe General Hospital Corporation, d/b/a MassachusettsK262293EVOLUTION MPX™ Total Knee SystemSuzhou Microport Orthorecon Co., Ltd.K262341b-ONE® Mobio™ Total Knee System Revision Cemented Tibial Augments, Stem Extensions and Press-Fit Stem ExtensionsB-One Ortho, Corp.K262130ATTUNE Revision Knee SystemDepuy Orthopaedics, Inc.K253961SK Knee SystemJust Medical Devices (Tianjin) Co., Ltd.

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.

↑