Home / 510(k) Clearances / K780890

510(k) K780890

CAPP TERMINAL DEVICE by Hosmer Dorrance Corp. — Product Code IQX

K780890 is an FDA 510(k) premarket notification submitted by Hosmer Dorrance Corp. for the device "CAPP TERMINAL DEVICE". The FDA issued a decision of Substantially Equivalent on June 13, 1978. The device falls under product code IQX (Hook, External Limb Component, Mechanical), a Class I device regulated under 21 CFR 890.3420. Hosmer Dorrance Corp. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 13, 1978
Date Received
May 31, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hook, External Limb Component, Mechanical
Device Class
Class I
Regulation Number
890.3420
Review Panel
PM
Submission Type

Other clearances by Hosmer Dorrance Corp.

  • K822632 — ELBOW PROSTHESIS (September 14, 1982)
  • K821704 — FRACTURE BRACING (June 24, 1982)
  • K801788 — HUMEROUS FRACTURE BRACE, ULNA FRACTURE (August 7, 1980)
  • K780891 — POST-OPERATIVE HIP ORTHOSIS (June 13, 1978)
  • K780892 — FRACTURE BRACING (June 13, 1978)
  • K761312 — ORTHOTIC BRACING (January 10, 1977)
  • K761314 — FLEXION-BRAKING KNEE-SHIN ASSEMBLY (January 10, 1977)
  • K761313 — 4-BAR KNEE-SHIN SET-UP (January 10, 1977)

FDA data resources