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FDA 510(k)

KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER

K-Number: K964752 · 1997-02-24

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1997-02-24
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1997-02-24 under 510(k) number K964752. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER?

KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER is a medical device that received FDA 510(k) clearance on 1997-02-24. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K964752.

When did KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER receive FDA 510(k) clearance?

KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER received FDA 510(k) clearance on 1997-02-24, under 510(k) number K964752.

Who is the listed applicant for KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER?

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

What is the FDA product code for KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER?

The FDA product code for KINEMATIC POSITIONING DEVICES; C-SPINE, KNEE,SHOULDER is LNH.

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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.

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