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FDA 510(k)

101 NEER TYPE SHOULDER

K-Number: K822771 · 1982-10-06

ApplicantIntermedics Orthopedics
Decision Date1982-10-06
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

101 NEER TYPE SHOULDER is the device name listed in this FDA 510(k) record. The listed applicant is Intermedics Orthopedics. It received FDA 510(k) clearance on 1982-10-06 under 510(k) number K822771. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 101 NEER TYPE SHOULDER?

101 NEER TYPE SHOULDER is a medical device that received FDA 510(k) clearance on 1982-10-06. The listed applicant is Intermedics Orthopedics. The 510(k) number is K822771.

When did 101 NEER TYPE SHOULDER receive FDA 510(k) clearance?

101 NEER TYPE SHOULDER received FDA 510(k) clearance on 1982-10-06, under 510(k) number K822771.

Who is the listed applicant for 101 NEER TYPE SHOULDER?

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

What is the FDA product code for 101 NEER TYPE SHOULDER?

The FDA product code for 101 NEER TYPE SHOULDER is HSD.

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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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