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)

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM

K-Number: K033810 · 2004-03-05

ApplicantCenterpulse Orthopedics, Inc.
Decision Date2004-03-05
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Centerpulse Orthopedics, Inc.. It received FDA 510(k) clearance on 2004-03-05 under 510(k) number K033810. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM?

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 2004-03-05. The listed applicant is Centerpulse Orthopedics, Inc.. The 510(k) number is K033810.

When did NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM receive FDA 510(k) clearance?

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM received FDA 510(k) clearance on 2004-03-05, under 510(k) number K033810.

Who is the listed applicant for NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM?

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

What is the FDA product code for NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM?

The FDA product code for NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM is HRY.

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 Centerpulse 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.

K033943ALPHA METASUL 28MM AND 32MM ACETABULAR INSERTS, STANDARD AND HOODEDK033634EPSILON METASUL 32MM ACETABULAR INSERTS, STANDARD AND HOODEDK040947DURASUL BIPOLARK033664MODIFICATION TO ALLOCLASSIC ZWEYMULLER SL OFFSET FEMORAL STEMK032348CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUPK030923EPSILON DURASUL CONSTRAINED ACETABULAR LINER

View all 10 devices →

Related Devices (Code: HRY)

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.

K193549SIGMA High Performance (HP) Partial Knee SystemDepuy Ireland UCK190633NanoOrtho NanoKnee® SystemNanoortho, LLCK152631MPO Total Knee Systems MR LabelingMicroport Orthopedics, Inc.K131167UNIVATIONAesculap Implant Systems, LLCK122277OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (OXFORD TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEMBiomet Manufacturing CorpK110415SIGNATURE PLANNER / SIGNATURE GUIDESMaterialise NV

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.

↑