FDA 510(k)

SCOLIOMETER

K-Number: K832494 · 1983-08-16

Decision Date1983-08-16

Product Code

DecisionSubstantially Equivalent

Device Summary

SCOLIOMETER 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 1983-08-16 under 510(k) number K832494. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOLIOMETER?

SCOLIOMETER is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K832494.

When did SCOLIOMETER receive FDA 510(k) clearance?

SCOLIOMETER received FDA 510(k) clearance on 1983-08-16, under 510(k) number K832494.

Who is the listed applicant for SCOLIOMETER?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Orthopedic Systems, Inc. as applicant

K952495ANCHORS AWAY SOFT TISSUE ATTACHMENT SYSTEM K920256SPINE MOTION ANALYZER WITH EMG K910736JACKSON MULTIPURPOSE OPERATING TABLE K910031PARK CITY SHOULDER POSITIONER K903938C FIT CUP K892503NUFFIELD TOTAL KNEE

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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.