510(k) K870083
- Device
- FERRAY EXTRACTOR
- Applicant
- TERRAY MANUFACTURING, INC.
- 510(k) number
- K870083
- Product code
- HWB
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1987-02-26
- Date received
- 1987-01-08
- Regulation
- 888.4540
- Classification name
- Extractor
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- RAY DESJARDINS
- Address
- 24 Mcgonigal St. W. Arnprior Ontario K7s 1l8 CA
FDA Registration Numbers#
- 1000517406
- 2249529
- 3010065126
- 3034525
- 9610809
- 3037407500
- 3009381600
- 3009241418
- 3009546990
- 3013564228
- 9616246
- 1056350
- 3015451162
- 3005739886
- 3015212339
- 3006846753
- 3007366790
- 1057425
- 8031020
- 3009971621
- 3005031160
- 3030989819
- 2134947
- 8010665
- 3015167917
- 1030489
- 9681642
- 1032347
- 3036756245
- 3004142400
- 3017397663
- 1827096
- 1226544
- 9611102
- 3010363503
- 9611503
- 1835251
- 3004774118
- 1834331
- 1834379
- 2249418
- 8010252
- 3010388970
- 3009051471
- 1043534
- 3008544874
- 8030607
- 3005641619
- 3006395932
- 3000270450
- 8043971
- 9616671
- 3002834291
- 3009165919
- 3000931034
- 3010536692
- 3012130008
- 3008455034
- 9612278
- 3010386387
- 3013875765
- 3004513872
- 1020279
- 3007125392
- 3005677016
- 3010039400
- 3011137372
- 3006809628
- 3007728266
- 3026311512
- 2132732
- 3010057495
- 3009887475
- 1720747
- 3002498892
- 3008650117
- 3009888740
- 3007420745
- 3010287737
- 3012131184
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HWB #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K873710 | MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350 | Arthropedics, Inc. | 1987-11-02 |
| K870844 | SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR | Warsaw Orthopedic, Inc. | 1987-03-13 |
| K801327 | THE EXTRACTOR I TM | The Anspach Effort, Inc. | 1980-06-09 |
| K780300 | HIP PLATE REMOVAL INSTRUMENT | Richard'S Medical Equip., Inc. | 1978-02-28 |
Legacy Summary#
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FDA Review#
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