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)

JACKSON MULTIPURPOSE OPERATING TABLE

K-Number: K910736 · 1991-05-21

ApplicantOrthopedic Systems, Inc.
Decision Date1991-05-21
Product CodeJEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JACKSON MULTIPURPOSE OPERATING TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Systems, Inc.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K910736. The device is classified under product code JEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JACKSON MULTIPURPOSE OPERATING TABLE?

JACKSON MULTIPURPOSE OPERATING TABLE is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K910736.

When did JACKSON MULTIPURPOSE OPERATING TABLE receive FDA 510(k) clearance?

JACKSON MULTIPURPOSE OPERATING TABLE received FDA 510(k) clearance on 1991-05-21, under 510(k) number K910736.

Who is the listed applicant for JACKSON MULTIPURPOSE OPERATING TABLE?

The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JACKSON MULTIPURPOSE OPERATING TABLE?

The FDA product code for JACKSON MULTIPURPOSE OPERATING TABLE is JEA.

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 Orthopedic Systems, Inc. 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.

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEMK920256SPINE MOTION ANALYZER WITH EMGK910031PARK CITY SHOULDER POSITIONERK903938C FIT CUPK892503NUFFIELD TOTAL KNEEK896678SILICONE PLUG

View all 95 devices →

Related Devices (Code: JEA)

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.

K953071STRYKER COMMAND2 OFFICE CONSOLEStryker InstrumentsK924094MEND APCMend Technologies, Inc.K911522ARTHROBOT(TM) WRIST HOLDER ACCESSORYAndronic Devices, Ltd.K900290SKYTRON MODEL 1100 AND MODEL 142Skytron, Div. the Kmw Group, Inc.K894789DMI 250 SERIES POWER SURGERY TABLEM.D. Intl., Inc.K881060OSI RIZZOLI TRAUMA TABLE (ELECTRIC VERSION)Orthopedic Systems, 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.

↑