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)

MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT

K-Number: K844482 · 1985-02-19

ApplicantAdvanced Biosearch Assn.
Decision Date1985-02-19
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biosearch Assn.. It received FDA 510(k) clearance on 1985-02-19 under 510(k) number K844482. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT?

MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT is a medical device that received FDA 510(k) clearance on 1985-02-19. The listed applicant is Advanced Biosearch Assn.. The 510(k) number is K844482.

When did MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT receive FDA 510(k) clearance?

MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT received FDA 510(k) clearance on 1985-02-19, under 510(k) number K844482.

Who is the listed applicant for MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT?

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

What is the FDA product code for MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT?

The FDA product code for MULLER TITANIUM BACKED ACETABULAR CUP COMPONENT is JDL.

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 Advanced Biosearch Assn. 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.

K905514AUTOGENESIS(TM) AUTOMATORK883888CATHSCANNER INTRAVASCULAR ULTRASONIC IMAGING SYST.K854770MARTIN LAMINAR OSTEOSYNTHESIS SYSTEMK855030CHAMPY BONE PLATES & BONE SCREWSK855031MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE PK853916P.M. HIP-FEMORAL PROSTHESIS

View all 22 devices →

Related Devices (Code: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, 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.

↑