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)

WEBER PERMALOCK

K-Number: K896669 · 1990-02-06

ApplicantAllo Pro Corp.
Decision Date1990-02-06
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

WEBER PERMALOCK is the device name listed in this FDA 510(k) record. The listed applicant is Allo Pro Corp.. It received FDA 510(k) clearance on 1990-02-06 under 510(k) number K896669. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WEBER PERMALOCK?

WEBER PERMALOCK is a medical device that received FDA 510(k) clearance on 1990-02-06. The listed applicant is Allo Pro Corp.. The 510(k) number is K896669.

When did WEBER PERMALOCK receive FDA 510(k) clearance?

WEBER PERMALOCK received FDA 510(k) clearance on 1990-02-06, under 510(k) number K896669.

Who is the listed applicant for WEBER PERMALOCK?

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

What is the FDA product code for WEBER PERMALOCK?

The FDA product code for WEBER PERMALOCK is LZO.

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 Allo Pro 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.

K901581GSB ELBOWK900425SURGICAL COTTON GLOVESK900392CENTERING PLUGK892644BIOLOX CERAMIC BALLK885049RS-CUP ACETABULAR PROSTHESISK864999KENNEDY STEM

View all 16 devices →

Related Devices (Code: LZO)

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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast 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.

↑