510(k) K770898
- Device
- FRACTURE CAST BRACE KIT, PLASTIC
- Applicant
- Chase Mfg. Co.
- 510(k) number
- K770898
- Product code
- HSP
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-07-21
- Date received
- 1977-05-16
- Regulation
- 888.5890
- Classification name
- Splint, Traction
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3002754225
- 8010099
- 8030607
- 3009148458
- 3005273623
- 1000560772
- 3007076137
- 3014368824
- 1026765
- 3010123014
- 1721819
- 3005621808
- 1526534
- 3017299525
- 3012777736
- 3016707060
- 3016704566
- 3006157842
- 3011657181
- 1000604079
- 3006089112
- 3007109661
- 2921578
- 3010729057
- 3023339256
- 1062671
- 1058584
- 3013524663
- 1043615
- 3043648115
- 3006750986
- 3009290468
- 3010452421
- 3010303097
- 3015194285
- 3005037196
- 3004547763
- 3007123908
- 3007084590
- 1528440
- 1036781
- 3003887292
- 8040278
- 3006943846
- 3016426842
- 1051550
- 3005024024
- 3023809973
- 3009605026
- 3007774549
- 3008395114
- 3013846070
- 3015378469
- 1836161
- 3043619977
- 1043214
- 9617759
- 3034669683
- 3011497619
- 3012309743
- 3021987422
- 3011280379
Source Documents#
510(k) summary PDF not indicated by FDA