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)

ORTHOSORB(R) ABSORBABLE PIN

K-Number: K901456 · 1990-08-15

ApplicantJohnson & Johnson International
Decision Date1990-08-15
Product CodeOVZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ORTHOSORB(R) ABSORBABLE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson International. It received FDA 510(k) clearance on 1990-08-15 under 510(k) number K901456. The device is classified under product code OVZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHOSORB(R) ABSORBABLE PIN?

ORTHOSORB(R) ABSORBABLE PIN is a medical device that received FDA 510(k) clearance on 1990-08-15. The listed applicant is Johnson & Johnson International. The 510(k) number is K901456.

When did ORTHOSORB(R) ABSORBABLE PIN receive FDA 510(k) clearance?

ORTHOSORB(R) ABSORBABLE PIN received FDA 510(k) clearance on 1990-08-15, under 510(k) number K901456.

Who is the listed applicant for ORTHOSORB(R) ABSORBABLE PIN?

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

What is the FDA product code for ORTHOSORB(R) ABSORBABLE PIN?

The FDA product code for ORTHOSORB(R) ABSORBABLE PIN is OVZ.

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 Johnson & Johnson International 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.

K965198ULTIMA TPS CEMENTED STEMK944937SYNTHETIC ABSORBABLE SUTUREK946245TIELLE* HYDROPOLYMER DRESSINGK942383DERMIVIEW CLEAR TAPEK922918BARRIER SAF-TE HYDROGEL DRAPEK923807P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS

View all 10 devices →

Related Devices (Code: OVZ)

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.

K111077ORTHOSORB RESORBABLE PINSDePuy Orthopaedics, 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.

↑