H-H HUNTER ACTIVE TENDON IMPLANT DC— 510(k) K872285

Name: FDA 510(k) clearance K872285
Creator: U.S. Food and Drug Administration
Published: 1987-09-28

Substantially Equivalent for Some Indications

Holter-Hausner Intl.

FDA 510(k) clearance K872285 for H-H HUNTER ACTIVE TENDON IMPLANT DC, Substantially Equivalent for Some Indications on 1987-09-28. Applicant: Holter-Hausner Intl.. Device class: 2.

Clearance details

Applicant: Holter-Hausner Intl.
Product code: Code HXA
Device class: Class 2
Regulation: 21 CFR 888.3025
Advisory panel: Orthopedic
Date received: 1987-06-16
Decision date: 1987-09-28
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Bridgeport, PA, US

Download summary PDF View on FDA.gov ↗

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K872284 — H-H HUNTER ACTIVE TENDON IMPLANT PC1987-09-28
K872293 — H-H HUNTER ACTIVE TENDON IMPLANT BC1987-09-28
K871351 — H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP1987-05-14

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