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)

ACETABULAR CUP PUSHER/IMPACTOR

K-Number: K885305 · 1989-02-08

ApplicantCobot Medical Corp.
Decision Date1989-02-08
Product CodeHXO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACETABULAR CUP PUSHER/IMPACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Cobot Medical Corp.. It received FDA 510(k) clearance on 1989-02-08 under 510(k) number K885305. The device is classified under product code HXO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR CUP PUSHER/IMPACTOR?

ACETABULAR CUP PUSHER/IMPACTOR is a medical device that received FDA 510(k) clearance on 1989-02-08. The listed applicant is Cobot Medical Corp.. The 510(k) number is K885305.

When did ACETABULAR CUP PUSHER/IMPACTOR receive FDA 510(k) clearance?

ACETABULAR CUP PUSHER/IMPACTOR received FDA 510(k) clearance on 1989-02-08, under 510(k) number K885305.

Who is the listed applicant for ACETABULAR CUP PUSHER/IMPACTOR?

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

What is the FDA product code for ACETABULAR CUP PUSHER/IMPACTOR?

The FDA product code for ACETABULAR CUP PUSHER/IMPACTOR is HXO.

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

Related Devices (Code: HXO)

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.

K803165ACETABULAR CEMENT COMPRESSORZimmer, Inc.K771072INSERTEO, META.-PHAL.&THUMB CARPO-METADepuy, 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.

↑