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)

BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID

K-Number: K854710 · 1986-04-16

ApplicantReloke Co.
Decision Date1986-04-16
Product CodeKNN
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID is the device name listed in this FDA 510(k) record. The listed applicant is Reloke Co.. It received FDA 510(k) clearance on 1986-04-16 under 510(k) number K854710. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID?

BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID is a medical device that received FDA 510(k) clearance on 1986-04-16. The listed applicant is Reloke Co.. The 510(k) number is K854710.

When did BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID receive FDA 510(k) clearance?

BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID received FDA 510(k) clearance on 1986-04-16, under 510(k) number K854710.

Who is the listed applicant for BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID?

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

What is the FDA product code for BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID?

The FDA product code for BOTTOMS-UP TM PELVIC SPINAL POSTURE-AID is KNN.

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

Related Devices (Code: KNN)

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.

K211919KISS Dynamic Back Support, KISS Dynamic Solid Drop SeatKinetic Innovative Seating System, LLCK942309DYNASTY U1-31 (GELL/CELL)Foley & LardnerK942311DYNASTY U1-33 AGMFoley & LardnerK942308DYNASTY GC 12400 (GELL/CELL)Foley & LardnerK942310DYNASTY GC 12550 (GELL/CELL)Foley & LardnerK942312ALDEN LINEAGE WHEELCHAIR CUSHIONLewis W. Ward

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.

↑