FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PASSIVE TENDON IMPLANT

K Number: K780320 · Decision Mar 17, 1978
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
10
Applicant Total
42
Review Days
21

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Basic Information

Device Name
PASSIVE TENDON IMPLANT
K Number
K780320
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3025
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Holter-Hausner Intl.
Date Received
February 24, 1978
Decision Date
March 17, 1978
Product Code
HXA
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HXA Prosthesis, Tendon, Passive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HXA), ordered by most recent decision date.

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Other Clearances by Holter-Hausner Intl.

K Number Device Name
K875287 H-H FLUSHING RESERVOIR
K874508 H-H EXTERNAL VENTRICULAR DRAINAGE COLLECTION BAG
K872285 H-H HUNTER ACTIVE TENDON IMPLANT DC
K872284 H-H HUNTER ACTIVE TENDON IMPLANT PC
K872293 H-H HUNTER ACTIVE TENDON IMPLANT BC
K871351 H-H HARRIS NEONATAL NASAL CANNULA SET FOR CPAP
K870660 H-H EXTERNAL VENTRICULAR DRAIN (EVD) COMP./SYSTEMS
K865075 H-H SUBGALEAL TROCAR
K853436 H-H HUNTER PASSIVE TENDON IMPLANT
K853437 H-H HUNTER TENDON ROD
Search all 42 clearances from Holter-Hausner Intl. →