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FDA 510(k)

TILLMAN HIPSURFACE REPLACEMENT

K-Number: K781490 · 1978-09-20

ApplicantWaldemar Link GmbH & Co. KG
Decision Date1978-09-20
Product CodeKXA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TILLMAN HIPSURFACE REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Waldemar Link GmbH & Co. KG. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781490. The device is classified under product code KXA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TILLMAN HIPSURFACE REPLACEMENT?

TILLMAN HIPSURFACE REPLACEMENT is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Waldemar Link GmbH & Co. KG. The 510(k) number is K781490.

When did TILLMAN HIPSURFACE REPLACEMENT receive FDA 510(k) clearance?

TILLMAN HIPSURFACE REPLACEMENT received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781490.

Who is the listed applicant for TILLMAN HIPSURFACE REPLACEMENT?

The FDA 510(k) record lists Waldemar Link GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TILLMAN HIPSURFACE REPLACEMENT?

The FDA product code for TILLMAN HIPSURFACE REPLACEMENT is KXA.

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Other records listing Waldemar Link GmbH & Co. KG as applicant

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Related Devices (Code: KXA)

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.

K201219Biocore9 Femoral Head Resurfacing ComponentBiocore9, LLCK092198CORMET CEMENTLESS RESURFACING FEMORAL HEADCorin USAK082673CONSERVE PRESSFIT FEMORAL COMPONENTWrightmedicaltechnologyincK071053RECAP HA PRESS-FIT FEMORAL RESURFACING HEADBiomet, Inc.K070292DUROM HIP RESURFACING SYSTEM, FEMORAL COMPONENTSZimmer GmbHK062960CONSERVE FEMORAL RESURFACING COMPONENTWrightmedicaltechnologyinc

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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