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

Unit, Traction, Hip, Non-Powered, Non-Penetrating

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

HSR is the FDA product code for Unit, Traction, Hip, Non-Powered, Non-Penetrating, 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 no recalls.

Classification record

Product code
HSR
Device name
Unit, Traction, Hip, Non-Powered, Non-Penetrating
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
0

Clearances, product code HSR

By decision year
1 clearance under product code HSR with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code HSR by decision year
YearClearances
19781

Applicants with the most clearances

Product code HSR
Applicants holding the most 510(k) clearances under product code HSR
ApplicantClearances
Orthopedic Equipment Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code