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)

KRONNER SACRAL PIN GUIDE

K-Number: K895172 · 1989-09-12

ApplicantKronner Medical
Decision Date1989-09-12
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KRONNER SACRAL PIN GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Medical. It received FDA 510(k) clearance on 1989-09-12 under 510(k) number K895172. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KRONNER SACRAL PIN GUIDE?

KRONNER SACRAL PIN GUIDE is a medical device that received FDA 510(k) clearance on 1989-09-12. The listed applicant is Kronner Medical. The 510(k) number is K895172.

When did KRONNER SACRAL PIN GUIDE receive FDA 510(k) clearance?

KRONNER SACRAL PIN GUIDE received FDA 510(k) clearance on 1989-09-12, under 510(k) number K895172.

Who is the listed applicant for KRONNER SACRAL PIN GUIDE?

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

What is the FDA product code for KRONNER SACRAL PIN GUIDE?

The FDA product code for KRONNER SACRAL PIN GUIDE is LXH.

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 Kronner Medical 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.

K894228KRONNER SPHERICAL CUTTERSK895171BLOOD GAS SAFETY SYRINGEK895173SKELETAL FIXATION PINK871248KRONNER COLLES-FOREARM EXTERNAL FIXATIONK871249KRONNER BI-PLANER TIBIA EXTERNAL FIXATIONK871247KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

View all 7 devices →

Related Devices (Code: LXH)

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.

K192873SX-One MicroKnifeSonex Health, Inc.K101609SELF RETAINING SOFT TISSUE RETRACTORKoros USA, Inc.K001507MICROPERFORATION INSTRUMENTSmith & Nephew, Inc.K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMOrthopedic Systems, Inc.K943873ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SYOrthomet, Inc.K944188SPINAL MARKERLeibinger L.P.

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.

↑