510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HSPClass I

Splint, Traction

21 CFR 888.5890 / Orthopedic
FDA source (opens on fda.gov)

HSP is the FDA product code for Splint, Traction, a class I device type, regulated under 21 CFR 888.5890. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and one recall.

Classification record

Product code
HSP
Device name
Splint, Traction
Regulation
21 CFR 888.5890
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
1

Clearances, product code HSP

By decision year
1 clearance under product code HSP with a decision year between 1977 and 1977, 1977 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HSP by decision year
YearClearances
19771

Applicants with the most clearances

Product code HSP
Applicants holding the most 510(k) clearances under product code HSP
ApplicantClearances
Chase Mfg. Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 63 companies shown, in name order